geneid | 11282 |
---|---|
ensemblid | ENSG00000161013.17 |
hgncid | 7048 |
symbol | MGAT4B |
name | alpha-1,3-mannosyl-glycoprotein 4-beta-N-acetylglucosaminyltransferase B |
refseq_nuc | NM_014275.5 |
refseq_prot | NP_055090.1 |
ensembl_nuc | ENST00000292591.12 |
ensembl_prot | ENSP00000292591.7 |
mane_status | MANE Select |
chr | chr5 |
start | 179797610 |
end | 179806866 |
strand | - |
ver | v1.2 |
region | chr5:179797610-179806866 |
region5000 | chr5:179792610-179811866 |
regionname0 | MGAT4B_chr5_179797610_179806866 |
regionname5000 | MGAT4B_chr5_179792610_179811866 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 548 | 395 | 92 | 74 | 171 | 14 | 42 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0002 | 0/0 | 548 | 6 | 0 | 0 | 6 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0003 | 0/0 | 548 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0004 | 0/0 | 548 | 2 | 1 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0005 | 0/0 | 548 | 2 | 0 | 0 | 0 | 0 | 2 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0006 | 0/0 | 548 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0007 | 0/0 | 548 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0008 | 0/0 | 548 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0009 | 0/0 | 548 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0010 | 0/0 | 548 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1647 | 347 | 53 | 71 | 166 | 14 | 41 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
c0002 | 0/0 | 1647 | 18 | 16 | 2 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
c0003 | 0/0 | 1647 | 16 | 15 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
c0004 | 0/0 | 1647 | 6 | 0 | 0 | 6 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
c0005 | 0/0 | 1647 | 5 | 5 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
c0006 | 0/0 | 1647 | 3 | 0 | 0 | 3 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
c0007 | 0/0 | 1647 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
c0008 | 0/0 | 1647 | 2 | 0 | 0 | 0 | 0 | 2 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
c0009 | 0/0 | 1647 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
c0010 | 0/0 | 1647 | 2 | 1 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
c0011 | 0/0 | 1647 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
c0012 | 0/0 | 1647 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
c0013 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
c0014 | 0/0 | 1647 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
c0015 | 0/0 | 1647 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
c0016 | 0/0 | 1647 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
c0017 | 0/0 | 1647 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
c0018 | 0/0 | 1647 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
c0019 | 0/0 | 1647 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 719 | 337 | 76 | 69 | 136 | 14 | 40 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
t0002 | 0/0 | 722 | 55 | 12 | 7 | 33 | 0 | 3 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
t0003 | 0/0 | 719 | 3 | 0 | 0 | 3 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
t0004 | 0/0 | 722 | 3 | 0 | 0 | 3 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
t0005 | 0/0 | 719 | 3 | 3 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
t0006 | 0/0 | 719 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
t0007 | 0/0 | 719 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
t0008 | 0/0 | 719 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
t0009 | 0/0 | 719 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
t0010 | 0/0 | 719 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
t0011 | 0/0 | 719 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
t0012 | 0/0 | 719 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
t0013 | 0/0 | 719 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
t0014 | 0/0 | 719 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 102 | 14 | 29 | 41 | 3 | 15 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0002 | 0/0 | 41 | 1 | 13 | 15 | 6 | 6 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0003 | 0/0 | 34 | 1 | 7 | 25 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0004 | 0/1 | 33 | 3 | 9 | 16 | 1 | 3 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0005 | 0/0 | 17 | 0 | 2 | 13 | 0 | 2 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0012 | 1/0 | 4 | 0 | 0 | 3 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0015 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | a0001 | c0001 | 1/1 | 347 | 53 | 71 | 166 | 14 | 41 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0002 | a0001 | c0002 | 0/0 | 18 | 16 | 2 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0003 | a0001 | c0003 | 0/0 | 16 | 15 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0005 | a0001 | c0005 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0006 | a0001 | c0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0009 | a0001 | c0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0013 | a0001 | c0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0014 | a0001 | c0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0016 | a0001 | c0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0019 | a0001 | c0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0002c0004 | a0002 | c0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0003c0007 | a0003 | c0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0004c0010 | a0004 | c0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0005c0008 | a0005 | c0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0006c0015 | a0006 | c0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0007c0012 | a0007 | c0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0008c0017 | a0008 | c0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0009c0011 | a0009 | c0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0010c0018 | a0010 | c0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | a0001 | c0001 | t0001 | 1/1 | 286 | 43 | 64 | 125 | 14 | 38 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 43 | 4 | 7 | 30 | 0 | 2 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0001t0003 | a0001 | c0001 | t0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0001t0006 | a0001 | c0001 | t0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0001t0007 | a0001 | c0001 | t0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0001t0008 | a0001 | c0001 | t0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0001t0010 | a0001 | c0001 | t0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0001t0011 | a0001 | c0001 | t0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0001t0012 | a0001 | c0001 | t0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0001t0013 | a0001 | c0001 | t0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0001t0014 | a0001 | c0001 | t0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0002t0001 | a0001 | c0002 | t0001 | 0/0 | 10 | 8 | 2 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0002t0002 | a0001 | c0002 | t0002 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0003t0001 | a0001 | c0003 | t0001 | 0/0 | 16 | 15 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0005t0001 | a0001 | c0005 | t0001 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0006t0002 | a0001 | c0006 | t0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0009t0001 | a0001 | c0009 | t0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0013t0001 | a0001 | c0013 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0014t0001 | a0001 | c0014 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0016t0001 | a0001 | c0016 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0001c0019t0001 | a0001 | c0019 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0002c0004t0001 | a0002 | c0004 | t0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0003c0007t0001 | a0003 | c0007 | t0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0004c0010t0001 | a0004 | c0010 | t0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0005c0008t0001 | a0005 | c0008 | t0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0005c0008t0002 | a0005 | c0008 | t0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0006c0015t0009 | a0006 | c0015 | t0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0007c0012t0001 | a0007 | c0012 | t0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0008c0017t0001 | a0008 | c0017 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0009c0011t0003 | a0009 | c0011 | t0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
a0010c0018t0001 | a0010 | c0018 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B | copy fasta |
actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 0/0 | 102 | 14 | 29 | 41 | 3 | 15 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 41 | 1 | 13 | 15 | 6 | 6 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/1 | 33 | 3 | 9 | 16 | 1 | 3 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/0 | 17 | 0 | 2 | 13 | 0 | 2 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 1/0 | 4 | 0 | 0 | 3 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0015 | a0001 | c0001 | t0001 | g0015 | 0/0 | 3 | 0 | 0 | 1 | 0 | 2 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0051 | a0001 | c0001 | t0001 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0055 | a0001 | c0001 | t0001 | g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0056 | a0001 | c0001 | t0001 | g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0060 | a0001 | c0001 | t0001 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0065 | a0001 | c0001 | t0001 | g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0102 | a0001 | c0001 | t0001 | g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0105 | a0001 | c0001 | t0001 | g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0106 | a0001 | c0001 | t0001 | g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0108 | a0001 | c0001 | t0001 | g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0110 | a0001 | c0001 | t0001 | g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0111 | a0001 | c0001 | t0001 | g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0112 | a0001 | c0001 | t0001 | g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0115 | a0001 | c0001 | t0001 | g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0117 | a0001 | c0001 | t0001 | g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0118 | a0001 | c0001 | t0001 | g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0119 | a0001 | c0001 | t0001 | g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0121 | a0001 | c0001 | t0001 | g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0122 | a0001 | c0001 | t0001 | g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0123 | a0001 | c0001 | t0001 | g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0125 | a0001 | c0001 | t0001 | g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0126 | a0001 | c0001 | t0001 | g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0127 | a0001 | c0001 | t0001 | g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0128 | a0001 | c0001 | t0001 | g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0129 | a0001 | c0001 | t0001 | g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0130 | a0001 | c0001 | t0001 | g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0131 | a0001 | c0001 | t0001 | g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0132 | a0001 | c0001 | t0001 | g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0001g0133 | a0001 | c0001 | t0001 | g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0002g0003 | a0001 | c0001 | t0002 | g0003 | 0/0 | 34 | 1 | 7 | 25 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0002g0039 | a0001 | c0001 | t0002 | g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0002g0041 | a0001 | c0001 | t0002 | g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0002g0042 | a0001 | c0001 | t0002 | g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0002g0044 | a0001 | c0001 | t0002 | g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0002g0045 | a0001 | c0001 | t0002 | g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0002g0046 | a0001 | c0001 | t0002 | g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0002g0048 | a0001 | c0001 | t0002 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0002g0049 | a0001 | c0001 | t0002 | g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0002g0050 | a0001 | c0001 | t0002 | g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0003g0019 | a0001 | c0001 | t0003 | g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0004g0022 | a0001 | c0001 | t0004 | g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0004g0047 | a0001 | c0001 | t0004 | g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0005g0023 | a0001 | c0001 | t0005 | g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0005g0054 | a0001 | c0001 | t0005 | g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0006g0020 | a0001 | c0001 | t0006 | g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0007g0035 | a0001 | c0001 | t0007 | g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0008g0124 | a0001 | c0001 | t0008 | g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0010g0120 | a0001 | c0001 | t0010 | g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0011g0085 | a0001 | c0001 | t0011 | g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0012g0069 | a0001 | c0001 | t0012 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0013g0114 | a0001 | c0001 | t0013 | g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0001t0014g0134 | a0001 | c0001 | t0014 | g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0002t0001g0010 | a0001 | c0002 | t0001 | g0010 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0002t0001g0017 | a0001 | c0002 | t0001 | g0017 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0002t0001g0058 | a0001 | c0002 | t0001 | g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0002t0001g0059 | a0001 | c0002 | t0001 | g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0002t0001g0109 | a0001 | c0002 | t0001 | g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0002t0002g0006 | a0001 | c0002 | t0002 | g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0002t0002g0021 | a0001 | c0002 | t0002 | g0021 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0002t0002g0043 | a0001 | c0002 | t0002 | g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0003t0001g0009 | a0001 | c0003 | t0001 | g0009 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0003t0001g0011 | a0001 | c0003 | t0001 | g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0003t0001g0024 | a0001 | c0003 | t0001 | g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0003t0001g0052 | a0001 | c0003 | t0001 | g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0003t0001g0057 | a0001 | c0003 | t0001 | g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0003t0001g0103 | a0001 | c0003 | t0001 | g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0003t0001g0104 | a0001 | c0003 | t0001 | g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0003t0001g0107 | a0001 | c0003 | t0001 | g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0005t0001g0018 | a0001 | c0005 | t0001 | g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0005t0001g0099 | a0001 | c0005 | t0001 | g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0005t0001g0100 | a0001 | c0005 | t0001 | g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0006t0002g0013 | a0001 | c0006 | t0002 | g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0009t0001g0037 | a0001 | c0009 | t0001 | g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0013t0001g0078 | a0001 | c0013 | t0001 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0014t0001g0113 | a0001 | c0014 | t0001 | g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0016t0001g0086 | a0001 | c0016 | t0001 | g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0001c0019t0001g0066 | a0001 | c0019 | t0001 | g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0002c0004t0001g0008 | a0002 | c0004 | t0001 | g0008 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0002c0004t0001g0091 | a0002 | c0004 | t0001 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0003c0007t0001g0030 | a0003 | c0007 | t0001 | g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0004c0010t0001g0098 | a0004 | c0010 | t0001 | g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0004c0010t0001g0101 | a0004 | c0010 | t0001 | g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0005c0008t0001g0084 | a0005 | c0008 | t0001 | g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0005c0008t0002g0040 | a0005 | c0008 | t0002 | g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0006c0015t0009g0062 | a0006 | c0015 | t0009 | g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0007c0012t0001g0082 | a0007 | c0012 | t0001 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0008c0017t0001g0116 | a0008 | c0017 | t0001 | g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0009c0011t0003g0038 | a0009 | c0011 | t0003 | g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
a0010c0018t0001g0072 | a0010 | c0018 | t0001 | g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MGAT4B_chr5_179792610_179811866 | MGAT4B |
sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | GBR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | GBR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | GBR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0097 | EUR | FIN | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | FIN | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01106 | hp1 | a0010 | c0018 | t0001 | g0072 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0017 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01243 | hp2 | a0001 | c0003 | t0001 | g0057 | AMR | PUR | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | IBS | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01884 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01884 | hp2 | a0004 | c0010 | t0001 | g0098 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01891 | hp2 | a0001 | c0005 | t0001 | g0018 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01934 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0050 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02055 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02083 | hp2 | a0001 | c0001 | t0010 | g0120 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02129 | hp2 | a0001 | c0019 | t0001 | g0066 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0103 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | CDX | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CDX | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02258 | hp1 | a0001 | c0005 | t0001 | g0018 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02280 | hp1 | a0008 | c0017 | t0001 | g0116 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02300 | hp2 | a0004 | c0010 | t0001 | g0101 | AMR | PEL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02451 | hp1 | a0001 | c0005 | t0001 | g0099 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02572 | hp2 | a0001 | c0005 | t0001 | g0100 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0052 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02698 | hp1 | a0001 | c0001 | t0014 | g0134 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02723 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02809 | hp2 | a0001 | c0002 | t0002 | g0006 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02818 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02895 | hp2 | a0001 | c0002 | t0002 | g0021 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02896 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02897 | hp1 | a0001 | c0003 | t0001 | g0011 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02897 | hp2 | a0001 | c0002 | t0002 | g0021 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0024 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02965 | hp1 | a0001 | c0013 | t0001 | g0078 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02965 | hp2 | a0001 | c0001 | t0013 | g0114 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02970 | hp2 | a0001 | c0009 | t0001 | g0037 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03041 | hp2 | a0001 | c0002 | t0002 | g0043 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0010 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0024 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03195 | hp1 | a0001 | c0009 | t0001 | g0037 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03225 | hp1 | a0001 | c0001 | t0006 | g0020 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03453 | hp1 | a0001 | c0002 | t0001 | g0058 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0023 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03516 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ESN | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0109 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03669 | hp1 | a0001 | c0016 | t0001 | g0086 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03704 | hp1 | a0005 | c0008 | t0002 | g0040 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | PJL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03942 | hp2 | a0005 | c0008 | t0001 | g0084 | SAS | BEB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | BEB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | STU | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0049 | SAS | STU | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | STU | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18522 | hp1 | a0001 | c0003 | t0001 | g0107 | AFR | YRI | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0054 | AFR | YRI | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18612 | hp1 | a0001 | c0014 | t0001 | g0113 | EAS | CHB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | CHB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | YRI | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18942 | hp2 | a0003 | c0007 | t0001 | g0030 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18947 | hp1 | a0001 | c0006 | t0002 | g0013 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18956 | hp2 | a0002 | c0004 | t0001 | g0091 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18961 | hp1 | a0003 | c0007 | t0001 | g0030 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18966 | hp2 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18974 | hp1 | a0001 | c0001 | t0007 | g0035 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18979 | hp2 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18993 | hp1 | a0001 | c0006 | t0002 | g0013 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18993 | hp2 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18997 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18997 | hp2 | a0001 | c0001 | t0004 | g0047 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19003 | hp2 | a0006 | c0015 | t0009 | g0062 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | LWK | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19043 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | LWK | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0011 | AFR | LWK | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19064 | hp2 | a0009 | c0011 | t0003 | g0038 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19067 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19070 | hp1 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19072 | hp1 | a0001 | c0001 | t0004 | g0022 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19078 | hp1 | a0001 | c0001 | t0008 | g0124 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19080 | hp1 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19081 | hp2 | a0001 | c0001 | t0007 | g0035 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19085 | hp1 | a0002 | c0004 | t0001 | g0008 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19086 | hp2 | a0007 | c0012 | t0001 | g0082 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19087 | hp1 | a0001 | c0006 | t0002 | g0013 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19087 | hp2 | a0001 | c0001 | t0012 | g0069 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19091 | hp2 | a0001 | c0001 | t0011 | g0085 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19240 | hp1 | a0001 | c0005 | t0001 | g0018 | AFR | YRI | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | YRI | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ASW | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | TSI | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | TSI | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | GIH | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | GIH | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02109 | hp1 | a0001 | c0002 | t0002 | g0006 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03471 | hp1 | a0001 | c0003 | t0001 | g0104 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG06807 | hp1 | a0001 | c0003 | t0001 | g0009 | AFR | USA | MGAT4B_chr5_179792610_179811866 | MGAT4B |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0020 | AFR | USA | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | USA | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | MGAT4B_chr5_179792610_179811866 | MGAT4B |
NA21309 | hp2 | a0001 | c0003 | t0001 | g0009 | AFR | LWK | MGAT4B_chr5_179792610_179811866 | MGAT4B |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0004 | REF | REF | MGAT4B_chr5_179792610_179811866 | MGAT4B |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0012 | REF | REF | MGAT4B_chr5_179792610_179811866 | MGAT4B |
chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:179798386
|
G | A | 1 | a0004 | 2 | HG01884.hp2 HG02300.hp2 |
missense_variant | MODERATE | c.1471C>T | p.Leu491Phe | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 13/15 | 1754/2365 | 1471/1647 | 491/548 | chr5 | 179798386 | ||
chr5:179798409
|
A | C | 1 | a0005 | 2 | HG03704.hp1 HG03942.hp2 |
missense_variant | MODERATE | c.1448T>G | p.Leu483Arg | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 13/15 | 1731/2365 | 1448/1647 | 483/548 | chr5 | 179798409 | ||
chr5:179798976
|
G | C | 1 | a0006 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.1295C>G | p.Ala432Gly | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 11/15 | 1578/2365 | 1295/1647 | 432/548 | chr5 | 179798976 | ||
chr5:179798977
|
C | G | 1 | a0006 | 1 | NA19003.hp2 | missense_variant | MODERATE | c.1294G>C | p.Ala432Pro | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 11/15 | 1577/2365 | 1294/1647 | 432/548 | chr5 | 179798977 | ||
chr5:179799549
|
T | G | 1 | a0007 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.998A>C | p.Asp333Ala | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/15 | 1281/2365 | 998/1647 | 333/548 | chr5 | 179799549 | ||
chr5:179799585
|
A | C | 1 | a0007 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.962T>G | p.Met321Arg | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/15 | 1245/2365 | 962/1647 | 321/548 | chr5 | 179799585 | ||
chr5:179799586
|
T | A | 1 | a0007 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.961A>T | p.Met321Leu | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/15 | 1244/2365 | 961/1647 | 321/548 | chr5 | 179799586 | ||
chr5:179799591
|
A | C | 1 | a0007 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.956T>G | p.Ile319Ser | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/15 | 1239/2365 | 956/1647 | 319/548 | chr5 | 179799591 | ||
chr5:179799624
|
T | G | 1 | a0007 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.923A>C | p.Lys308Thr | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/15 | 1206/2365 | 923/1647 | 308/548 | chr5 | 179799624 | ||
chr5:179799959
|
A | C | 1 | a0007 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.905T>G | p.Phe302Cys | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 8/15 | 1188/2365 | 905/1647 | 302/548 | chr5 | 179799959 | ||
chr5:179800031
|
C | G | 1 | a0007 | 1 | NA19086.hp2 | missense_variant | MODERATE | c.833G>C | p.Ser278Thr | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 8/15 | 1116/2365 | 833/1647 | 278/548 | chr5 | 179800031 | ||
chr5:179800040
|
T | C | 1 | a0008 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.824A>G | p.Asn275Ser | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 8/15 | 1107/2365 | 824/1647 | 275/548 | chr5 | 179800040 | ||
chr5:179800213
|
C | T | 1 | a0009 | 1 | NA19064.hp2 | missense_variant | MODERATE | c.766G>A | p.Ala256Thr | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 7/15 | 1049/2365 | 766/1647 | 256/548 | chr5 | 179800213 | ||
chr5:179801559
|
G | T | 1 | a0003 | 2 | NA18942.hp2 NA18961.hp1 |
missense_variant | MODERATE | c.419C>A | p.Thr140Asn | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 3/15 | 702/2365 | 419/1647 | 140/548 | chr5 | 179801559 | ||
chr5:179801641
|
G | A | 1 | a0010 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.337C>T | p.Pro113Ser | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 3/15 | 620/2365 | 337/1647 | 113/548 | chr5 | 179801641 | ||
chr5:179801891
|
T | C | 1 | a0002 | 6 | NA18956.hp2 NA18979.hp2 NA18993.hp2 others(3): Show |
missense_variant | MODERATE | c.176A>G | p.Lys59Arg | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 2/15 | 459/2365 | 176/1647 | 59/548 | chr5 | 179801891 |
chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:179798978
|
G | A | 1 | a0001c0016 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.1293C>T | p.Ala431Ala | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 11/15 | 1576/2365 | 1293/1647 | 431/548 | chr5 | 179798978 | ||
chr5:179798978
|
G | C | 1 | a0006c0015 | 1 | NA19003.hp2 | synonymous_variant | LOW | c.1293C>G | p.Ala431Ala | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 11/15 | 1576/2365 | 1293/1647 | 431/548 | chr5 | 179798978 | ||
chr5:179799074
|
C | T | 1 | a0001c0014 | 1 | NA18612.hp1 | synonymous_variant | LOW | c.1197G>A | p.Pro399Pro | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 11/15 | 1480/2365 | 1197/1647 | 399/548 | chr5 | 179799074 | ||
chr5:179799518
|
G | A | 1 | a0001c0002 | 18 | HG01243.hp1 HG01884.hp1 HG01934.hp1 others(15): Show |
synonymous_variant | LOW | c.1029C>T | p.Pro343Pro | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/15 | 1312/2365 | 1029/1647 | 343/548 | chr5 | 179799518 | ||
chr5:179799620
|
C | T | 1 | a0001c0013 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.927G>A | p.Ser309Ser | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/15 | 1210/2365 | 927/1647 | 309/548 | chr5 | 179799620 | ||
chr5:179801430
|
C | T | 1 | a0001c0006 | 3 | NA18947.hp1 NA18993.hp1 NA19087.hp1 |
synonymous_variant | LOW | c.462G>A | p.Glu154Glu | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 4/15 | 745/2365 | 462/1647 | 154/548 | chr5 | 179801430 | ||
chr5:179801585
|
G | A | 1 | a0001c0009 | 2 | HG02970.hp2 HG03195.hp1 |
synonymous_variant | LOW | c.393C>T | p.Pro131Pro | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 3/15 | 676/2365 | 393/1647 | 131/548 | chr5 | 179801585 | ||
chr5:179801623
|
G | A | 2 | a0001c0002a0001c0003 | 34 | HG01243.hp1 HG01243.hp2 HG01884.hp1 others(31): Show |
synonymous_variant | LOW | c.355C>T | p.Leu119Leu | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 3/15 | 638/2365 | 355/1647 | 119/548 | chr5 | 179801623 | ||
chr5:179801893
|
G | C | 2 | a0001c0005a0004c0010 | 7 | HG01884.hp2 HG01891.hp2 HG02258.hp1 others(4): Show |
synonymous_variant | LOW | c.174C>G | p.Leu58Leu | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 2/15 | 457/2365 | 174/1647 | 58/548 | chr5 | 179801893 | ||
chr5:179801926
|
G | A | 1 | a0001c0019 | 1 | HG02129.hp2 | synonymous_variant | LOW | c.141C>T | p.Arg47Arg | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 2/15 | 424/2365 | 141/1647 | 47/548 | chr5 | 179801926 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:179797680
|
G | A | 1 | a0001c0001t0005 | 3 | HG03209.hp2 HG03453.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*365C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 365 | chr5 | 179797680 | |||||
chr5:179797708
|
A | G | 1 | a0001c0001t0010 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*337T>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 337 | chr5 | 179797708 | |||||
chr5:179797750
|
G | C | 1 | a0001c0001t0008 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*295C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 295 | chr5 | 179797750 | |||||
chr5:179797751
|
C | G | 1 | a0001c0001t0008 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*294G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 294 | chr5 | 179797751 | |||||
chr5:179797784
|
C | A | 1 | a0001c0001t0011 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*261G>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 261 | chr5 | 179797784 | |||||
chr5:179797796
|
G | A | 2 | a0001c0001t0004a0001c0001t0012 | 4 | NA18966.hp2 NA18997.hp2 NA19072.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*249C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 249 | chr5 | 179797796 | |||||
chr5:179797857
|
G | A | 1 | a0001c0001t0014 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*188C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 188 | chr5 | 179797857 | |||||
chr5:179797863
|
C | G | 1 | a0006c0015t0009 | 1 | NA19003.hp2 | 3_prime_UTR_variant | MODIFIER | c.*182G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 182 | chr5 | 179797863 | |||||
chr5:179797945
|
T | G | 1 | a0001c0001t0008 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*100A>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 100 | chr5 | 179797945 | |||||
chr5:179797949
|
C | G | 1 | a0001c0001t0008 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*96G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 96 | chr5 | 179797949 | |||||
chr5:179797950
|
G | A | 1 | a0001c0001t0013 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*95C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 95 | chr5 | 179797950 | |||||
chr5:179797976
|
G | A | 1 | a0001c0001t0007 | 2 | NA18974.hp1 NA19081.hp2 |
3_prime_UTR_variant | MODIFIER | c.*69C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 15/15 | 69 | chr5 | 179797976 | |||||
chr5:179806663
|
A | AGGC | 5 | a0001c0001t0002a0001c0001t0004a0001c0002t0002others(2): Show | 58 | HG00408.hp2 HG00558.hp2 HG00609.hp1 others(55): Show |
5_prime_UTR_variant | MODIFIER | c.-83_-81dupGCC | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/15 | 81 | chr5 | 179806663 | |||||
chr5:179806666
|
C | G | 1 | a0001c0001t0006 | 2 | HG03225.hp1 HG06807.hp2 |
5_prime_UTR_variant | MODIFIER | c.-83G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/15 | 83 | chr5 | 179806666 | |||||
chr5:179806725
|
C | T | 2 | a0001c0001t0003a0009c0011t0003 | 3 | NA18950.hp2 NA18997.hp1 NA19064.hp2 |
5_prime_UTR_variant | MODIFIER | c.-142G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/15 | 142 | chr5 | 179806725 | |||||
chr5:179806740
|
G | A | 1 | a0001c0001t0014 | 1 | HG02698.hp1 | 5_prime_UTR_variant | MODIFIER | c.-157C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/15 | 157 | chr5 | 179806740 |
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_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:179798099
|
C | A | 4 | a0001c0005t0001g0099a0001c0005t0001g0100a0004c0010t0001g0098others(1): Show | 4 | HG01884.hp2 HG02300.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1624-31G>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 14/14 | chr5 | 179798099 | ||||||
chr5:179798324
|
G | A | 4 | a0001c0001t0001g0032a0001c0001t0001g0067a0001c0003t0001g0103others(1): Show | 7 | HG01433.hp1 HG01891.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.1510+23C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 13/14 | chr5 | 179798324 | ||||||
chr5:179798480
|
G | A | 3 | a0001c0001t0001g0032a0001c0001t0001g0067a0001c0005t0001g0018 | 6 | HG01433.hp1 HG01891.hp2 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.1422+33C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 12/14 | chr5 | 179798480 | ||||||
chr5:179798499
|
C | A | 4 | a0001c0005t0001g0099a0001c0005t0001g0100a0004c0010t0001g0098others(1): Show | 4 | HG01884.hp2 HG02300.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1422+14G>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 12/14 | chr5 | 179798499 | ||||||
chr5:179798504
|
C | T | 5 | a0001c0001t0001g0056a0001c0003t0001g0009a0001c0003t0001g0024others(2): Show | 10 | HG01243.hp2 HG02630.hp1 HG02922.hp2 others(7): Show |
intron_variant | MODIFIER | c.1422+9G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 12/14 | chr5 | 179798504 | ||||||
chr5:179798768
|
C | G | 8 | a0001c0002t0001g0010a0001c0002t0001g0017a0001c0002t0001g0058others(5): Show | 18 | HG01243.hp1 HG01884.hp1 HG01934.hp1 others(15): Show |
intron_variant | MODIFIER | c.1343+160G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 11/14 | chr5 | 179798768 | ||||||
chr5:179798811
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0067 | 3 | HG01433.hp1 HG02040.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.1343+117G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 11/14 | chr5 | 179798811 | ||||||
chr5:179798814
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1343+114C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 11/14 | chr5 | 179798814 | ||||||
chr5:179798830
|
G | A | 1 | a0001c0001t0005g0023 | 2 | HG03209.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1343+98C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 11/14 | chr5 | 179798830 | ||||||
chr5:179798912
|
T | C | 3 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0070 | 3 | NA18974.hp2 NA19055.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1343+16A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 11/14 | chr5 | 179798912 | ||||||
chr5:179799161
|
G | C | 1 | a0001c0003t0001g0107 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1150-40C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 10/14 | chr5 | 179799161 | ||||||
chr5:179799188
|
T | A | 1 | a0001c0001t0001g0087 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1149+15A>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 10/14 | chr5 | 179799188 | ||||||
chr5:179799341
|
G | A | 2 | a0001c0001t0001g0064a0001c0001t0001g0126 | 2 | NA18968.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1042-31C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/14 | chr5 | 179799341 | ||||||
chr5:179799365
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1042-55C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/14 | chr5 | 179799365 | ||||||
chr5:179799393
|
C | T | 1 | a0001c0001t0001g0083 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1042-83G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/14 | chr5 | 179799393 | ||||||
chr5:179799464
|
C | T | 4 | a0001c0001t0001g0032a0001c0001t0001g0067a0001c0003t0001g0103others(1): Show | 7 | HG01433.hp1 HG01891.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.1041+42G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 9/14 | chr5 | 179799464 | ||||||
chr5:179799639
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG02622.hp2 | splice_region_variant&intron_variant | LOW | c.911-3C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 8/14 | chr5 | 179799639 | ||||||
chr5:179799703
|
C | T | 3 | a0001c0001t0001g0034a0001c0001t0001g0128a0001c0009t0001g0037 | 5 | HG02257.hp1 HG02723.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.911-67G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 8/14 | chr5 | 179799703 | ||||||
chr5:179799774
|
T | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0096others(2): Show | 10 | HG02145.hp1 HG02572.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.911-138A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 8/14 | chr5 | 179799774 | ||||||
chr5:179799786
|
ACATGTCT others(23): Show |
A | 5 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0096others(2): Show | 10 | HG02145.hp1 HG02572.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.910+138_911-151del others(30): Show |
MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 8/14 | chr5 | 179799786 | ||||||
chr5:179799847
|
A | T | 1 | a0007c0012t0001g0082 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.910+107T>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 8/14 | chr5 | 179799847 | ||||||
chr5:179799850
|
G | C | 1 | a0007c0012t0001g0082 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.910+104C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 8/14 | chr5 | 179799850 | ||||||
chr5:179799915
|
G | A | 1 | a0001c0001t0001g0071 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.910+39C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 8/14 | chr5 | 179799915 | ||||||
chr5:179800096
|
G | C | 1 | a0001c0001t0001g0081 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.796-28C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 7/14 | chr5 | 179800096 | ||||||
chr5:179800097
|
C | G | 1 | a0001c0001t0001g0081 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.796-29G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 7/14 | chr5 | 179800097 | ||||||
chr5:179800099
|
G | C | 15 | a0001c0001t0001g0032a0001c0001t0001g0056a0001c0001t0001g0060others(12): Show | 24 | HG01243.hp2 HG01433.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.796-31C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 7/14 | chr5 | 179800099 | ||||||
chr5:179800129
|
T | TCGCAGGG others(8): Show |
4 | a0001c0005t0001g0099a0001c0005t0001g0100a0004c0010t0001g0098others(1): Show | 4 | HG01884.hp2 HG02300.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.795+40_795+54dupCC others(13): Show |
MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 7/14 | chr5 | 179800129 | ||||||
chr5:179800146
|
G | A | 1 | a0001c0001t0001g0031 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.795+38C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 7/14 | chr5 | 179800146 | ||||||
chr5:179800154
|
G | A | 15 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0029others(12): Show | 62 | HG00099.hp1 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.795+30C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 7/14 | chr5 | 179800154 | ||||||
chr5:179800274
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.720-15C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 6/14 | chr5 | 179800274 | ||||||
chr5:179800286
|
G | T | 40 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(37): Show | 106 | HG00140.hp1 HG00597.hp1 HG00733.hp1 others(103): Show |
intron_variant | MODIFIER | c.720-27C>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 6/14 | chr5 | 179800286 | ||||||
chr5:179800307
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.720-48A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 6/14 | chr5 | 179800307 | ||||||
chr5:179800327
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.720-68G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 6/14 | chr5 | 179800327 | ||||||
chr5:179800398
|
G | C | 4 | a0001c0001t0001g0007a0001c0001t0001g0096a0001c0001t0001g0118others(1): Show | 8 | HG02145.hp1 HG02572.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.719+86C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 6/14 | chr5 | 179800398 | ||||||
chr5:179800616
|
T | C | 1 | a0001c0001t0006g0020 | 2 | HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.606-19A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 5/14 | chr5 | 179800616 | ||||||
chr5:179800622
|
G | A | 1 | a0001c0001t0001g0090 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.606-25C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 5/14 | chr5 | 179800622 | ||||||
chr5:179800701
|
C | A | 2 | a0001c0002t0001g0109a0008c0017t0001g0116 | 2 | HG02280.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.606-104G>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 5/14 | chr5 | 179800701 | ||||||
chr5:179800826
|
A | G | 1 | a0001c0001t0001g0016 | 3 | HG02055.hp2 HG02976.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.605+81T>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 5/14 | chr5 | 179800826 | ||||||
chr5:179800844
|
G | T | 1 | a0001c0005t0001g0099 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.605+63C>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 5/14 | chr5 | 179800844 | ||||||
chr5:179800847
|
AGCACAAC others(20): Show |
A | 1 | a0002c0004t0001g0091 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.605+33_605+59delGG others(25): Show |
MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 5/14 | chr5 | 179800847 | ||||||
chr5:179800865
|
G | A | 10 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0003t0001g0009others(7): Show | 15 | HG01243.hp2 HG01884.hp2 HG02300.hp2 others(12): Show |
intron_variant | MODIFIER | c.605+42C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 5/14 | chr5 | 179800865 | ||||||
chr5:179801011
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.559-58C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 4/14 | chr5 | 179801011 | ||||||
chr5:179801018
|
G | A | 1 | a0001c0001t0006g0020 | 2 | HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.559-65C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 4/14 | chr5 | 179801018 | ||||||
chr5:179801149
|
C | CG | 7 | a0001c0001t0001g0015a0001c0001t0001g0061a0001c0001t0001g0068others(4): Show | 9 | HG01884.hp2 HG02523.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.558+184dupC | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 4/14 | chr5 | 179801149 | ||||||
chr5:179801150
|
G | A | 2 | a0001c0003t0001g0103a0001c0005t0001g0018 | 4 | HG01891.hp2 HG02145.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.558+184C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 4/14 | chr5 | 179801150 | ||||||
chr5:179801162
|
TA | T | 4 | a0001c0001t0001g0007a0001c0001t0001g0027a0001c0001t0001g0096others(1): Show | 9 | HG02145.hp1 HG02572.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.558+171delT | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 4/14 | chr5 | 179801162 | ||||||
chr5:179801173
|
G | A | 1 | a0001c0003t0001g0103 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.558+161C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 4/14 | chr5 | 179801173 | ||||||
chr5:179801215
|
C | G | 1 | a0001c0013t0001g0078 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.558+119G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 4/14 | chr5 | 179801215 | ||||||
chr5:179801473
|
G | A | 2 | a0001c0001t0001g0117a0001c0001t0001g0130 | 2 | HG01192.hp1 HG01261.hp1 |
splice_region_variant&intron_variant | LOW | c.425-6C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 3/14 | chr5 | 179801473 | ||||||
chr5:179801478
|
C | T | 1 | a0001c0002t0002g0021 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.425-11G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 3/14 | chr5 | 179801478 | ||||||
chr5:179801501
|
T | C | 2 | a0001c0001t0006g0020a0001c0003t0001g0103 | 3 | HG02145.hp2 HG03225.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.425-34A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 3/14 | chr5 | 179801501 | ||||||
chr5:179801522
|
C | A | 2 | a0001c0003t0001g0011a0001c0003t0001g0052 | 5 | HG02055.hp1 HG02647.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.424+32G>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 3/14 | chr5 | 179801522 | ||||||
chr5:179802005
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.98-36A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802005 | ||||||
chr5:179802032
|
G | A | 1 | a0001c0001t0001g0014 | 3 | HG00733.hp2 HG00741.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.98-63C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802032 | ||||||
chr5:179802039
|
A | C | 6 | a0001c0001t0001g0056a0001c0001t0001g0060a0001c0003t0001g0009others(3): Show | 11 | HG01243.hp2 HG02630.hp1 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.98-70T>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802039 | ||||||
chr5:179802151
|
A | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0128a0001c0001t0006g0020others(1): Show | 8 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.98-182T>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802151 | ||||||
chr5:179802296
|
G | A | 1 | a0001c0003t0001g0057 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.98-327C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802296 | ||||||
chr5:179802303
|
T | C | 1 | a0001c0009t0001g0037 | 2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.98-334A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802303 | ||||||
chr5:179802315
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.98-346C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802315 | ||||||
chr5:179802348
|
G | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0128a0001c0001t0006g0020 | 5 | HG02257.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.98-379C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802348 | ||||||
chr5:179802367
|
G | A | 1 | a0001c0002t0001g0059 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.98-398C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802367 | ||||||
chr5:179802396
|
T | C | 1 | a0001c0001t0001g0094 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.98-427A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802396 | ||||||
chr5:179802419
|
G | A | 1 | a0001c0009t0001g0037 | 2 | HG02970.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.98-450C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802419 | ||||||
chr5:179802464
|
C | CG | 7 | a0001c0001t0001g0056a0001c0001t0001g0077a0001c0001t0001g0123others(4): Show | 12 | HG01243.hp2 HG02630.hp1 HG02922.hp2 others(9): Show |
intron_variant | MODIFIER | c.98-496dupC | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802464 | ||||||
chr5:179802641
|
G | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0110 | 2 | HG00140.hp2 HG00735.hp1 |
intron_variant | MODIFIER | c.98-672C>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802641 | ||||||
chr5:179802649
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.98-680G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802649 | ||||||
chr5:179802688
|
T | A | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.98-719A>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802688 | ||||||
chr5:179802717
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.98-748A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802717 | ||||||
chr5:179802767
|
C | T | 1 | a0001c0001t0001g0025 | 2 | NA19000.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.98-798G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802767 | ||||||
chr5:179802817
|
G | A | 1 | a0001c0001t0001g0029 | 2 | NA18970.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.98-848C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802817 | ||||||
chr5:179802987
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0067 | 5 | HG01433.hp1 HG02040.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.98-1018G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179802987 | ||||||
chr5:179803238
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.98-1269G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803238 | ||||||
chr5:179803291
|
C | G | 1 | a0001c0002t0001g0058 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.98-1322G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803291 | ||||||
chr5:179803320
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.98-1351G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803320 | ||||||
chr5:179803321
|
T | C | 44 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(41): Show | 138 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.98-1352A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803321 | ||||||
chr5:179803448
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.98-1479C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803448 | ||||||
chr5:179803529
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.98-1560C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803529 | ||||||
chr5:179803556
|
C | A | 3 | a0001c0001t0001g0034a0001c0001t0001g0128a0001c0001t0006g0020 | 5 | HG02257.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.98-1587G>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803556 | ||||||
chr5:179803598
|
C | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0111 | 2 | HG03704.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.98-1629G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803598 | ||||||
chr5:179803617
|
G | C | 1 | a0001c0001t0001g0034 | 2 | HG02257.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.98-1648C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803617 | ||||||
chr5:179803669
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.98-1700C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803669 | ||||||
chr5:179803860
|
T | C | 1 | a0001c0001t0001g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.98-1891A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803860 | ||||||
chr5:179803892
|
T | G | 1 | a0001c0001t0001g0073 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.98-1923A>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803892 | ||||||
chr5:179803939
|
G | T | 1 | a0001c0001t0002g0046 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.98-1970C>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179803939 | ||||||
chr5:179804248
|
T | G | 54 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0016others(51): Show | 202 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.97+2239A>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179804248 | ||||||
chr5:179804255
|
A | G | 1 | a0001c0001t0002g0044 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.97+2232T>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179804255 | ||||||
chr5:179804257
|
A | ATCAGGCC others(43): Show |
1 | a0001c0001t0001g0110 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.97+2180_97+2229dup others(50): Show |
MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179804257 | ||||||
chr5:179804353
|
A | G | 3 | a0001c0001t0001g0034a0001c0001t0001g0128a0001c0001t0006g0020 | 5 | HG02257.hp1 HG02723.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+2134T>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179804353 | ||||||
chr5:179804424
|
G | A | 1 | a0001c0001t0001g0036 | 2 | NA18943.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.97+2063C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179804424 | ||||||
chr5:179804554
|
G | A | 4 | a0001c0005t0001g0099a0001c0005t0001g0100a0004c0010t0001g0098others(1): Show | 4 | HG01884.hp2 HG02300.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+1933C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179804554 | ||||||
chr5:179804600
|
G | A | 1 | a0001c0001t0001g0033 | 2 | HG00621.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.97+1887C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179804600 | ||||||
chr5:179804753
|
G | A | 1 | a0001c0001t0001g0121 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.97+1734C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179804753 | ||||||
chr5:179804884
|
C | T | 10 | a0001c0002t0001g0010a0001c0002t0001g0017a0001c0002t0001g0058others(7): Show | 23 | HG01243.hp1 HG01884.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.97+1603G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179804884 | ||||||
chr5:179804907
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.97+1580C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179804907 | ||||||
chr5:179805064
|
A | T | 2 | a0001c0005t0001g0018a0001c0009t0001g0037 | 5 | HG01891.hp2 HG02258.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+1423T>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805064 | ||||||
chr5:179805342
|
A | C | 1 | a0001c0001t0001g0123 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.97+1145T>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805342 | ||||||
chr5:179805387
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.97+1100C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805387 | ||||||
chr5:179805603
|
T | C | 5 | a0001c0001t0001g0034a0001c0001t0001g0128a0001c0001t0006g0020others(2): Show | 10 | HG01891.hp2 HG02257.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.97+884A>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805603 | ||||||
chr5:179805780
|
G | A | 1 | a0001c0003t0001g0103 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.97+707C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805780 | ||||||
chr5:179805825
|
G | A | 1 | a0001c0003t0001g0104 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.97+662C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805825 | ||||||
chr5:179805833
|
G | C | 1 | a0001c0001t0001g0105 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.97+654C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805833 | ||||||
chr5:179805866
|
G | C | 1 | a0001c0001t0001g0106 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.97+621C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805866 | ||||||
chr5:179805966
|
G | A | 7 | a0001c0001t0001g0056a0001c0003t0001g0009a0001c0003t0001g0024others(4): Show | 15 | HG01243.hp2 HG01891.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.97+521C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805966 | ||||||
chr5:179805976
|
GCCTC | G | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(91): Show | 296 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.97+507_97+510delGA others(2): Show |
MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805976 | ||||||
chr5:179805977
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.97+510G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805977 | ||||||
chr5:179805993
|
C | T | 3 | a0001c0001t0001g0056a0001c0003t0001g0024a0001c0003t0001g0057 | 4 | HG01243.hp2 HG02922.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+494G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179805993 | ||||||
chr5:179806106
|
T | TG | 10 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0126others(7): Show | 11 | HG01192.hp1 HG02015.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.97+380dupC | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179806106 | ||||||
chr5:179806140
|
C | CG | 4 | a0001c0001t0001g0053a0001c0001t0001g0055a0001c0001t0005g0023others(1): Show | 5 | HG03195.hp2 HG03209.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+346dupC | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179806140 | ||||||
chr5:179806172
|
G | A | 2 | a0001c0005t0001g0018a0001c0009t0001g0037 | 5 | HG01891.hp2 HG02258.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+315C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179806172 | ||||||
chr5:179806213
|
C | T | 1 | a0001c0003t0001g0052 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.97+274G>A | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179806213 | ||||||
chr5:179806273
|
G | A | 2 | a0001c0001t0001g0131a0001c0001t0001g0132 | 2 | HG02074.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.97+214C>T | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179806273 | ||||||
chr5:179806292
|
C | G | 1 | a0001c0001t0001g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.97+195G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179806292 | ||||||
chr5:179806295
|
G | C | 1 | a0001c0001t0001g0133 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.97+192C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179806295 | ||||||
chr5:179806371
|
G | C | 1 | a0001c0001t0001g0051 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.97+116C>G | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179806371 | ||||||
chr5:179806372
|
C | G | 1 | a0001c0001t0001g0051 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.97+115G>C | MGAT4B | ENSG00000161013.17 | transcript | ENST00000292591.12 | protein_coding | 1/14 | chr5 | 179806372 |