geneid | 23324 |
---|---|
ensemblid | ENSG00000013288.9 |
hgncid | 29623 |
symbol | MAN2B2 |
name | mannosidase alpha class 2B member 2 |
refseq_nuc | NM_015274.3 |
refseq_prot | NP_056089.1 |
ensembl_nuc | ENST00000285599.8 |
ensembl_prot | ENSP00000285599.3 |
mane_status | MANE Select |
chr | chr4 |
start | 6575189 |
end | 6623362 |
strand | + |
ver | v1.2 |
region | chr4:6575189-6623362 |
region5000 | chr4:6570189-6628362 |
regionname0 | MAN2B2_chr4_6575189_6623362 |
regionname5000 | MAN2B2_chr4_6570189_6628362 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1009 | 133 | 5 | 22 | 89 | 3 | 14 | 67 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002 | 0/1 | 1009 | 126 | 25 | 25 | 56 | 5 | 14 | 37 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0003 | 0/0 | 1009 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0004 | 0/0 | 1009 | 9 | 1 | 7 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0005 | 0/0 | 1009 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0006 | 0/0 | 1009 | 5 | 3 | 0 | 1 | 0 | 1 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0007 | 0/0 | 1009 | 5 | 1 | 1 | 2 | 1 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0008 | 1/0 | 1009 | 5 | 3 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0009 | 0/0 | 1009 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0010 | 0/0 | 1009 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0011 | 0/0 | 1009 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0012 | 0/0 | 1009 | 3 | 0 | 0 | 0 | 1 | 2 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0013 | 0/0 | 1009 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0014 | 0/0 | 1009 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0015 | 0/0 | 1009 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0016 | 0/0 | 1009 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0017 | 0/0 | 1009 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0018 | 0/0 | 1009 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0019 | 0/0 | 1009 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0020 | 0/0 | 1009 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0021 | 0/0 | 1009 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0022 | 0/0 | 1009 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0023 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0024 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0025 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0026 | 0/0 | 1009 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0027 | 0/0 | 1009 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0028 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0029 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0030 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0031 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0032 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0033 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0034 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0035 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0036 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0037 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0038 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0039 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0040 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0041 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0042 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0043 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0044 | 0/0 | 1009 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 3030 | 107 | 2 | 22 | 72 | 2 | 9 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0002 | 0/1 | 3030 | 98 | 11 | 22 | 49 | 3 | 12 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0003 | 0/0 | 3030 | 22 | 1 | 0 | 15 | 1 | 5 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0004 | 0/0 | 3030 | 21 | 11 | 2 | 4 | 2 | 2 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0005 | 0/0 | 3030 | 9 | 1 | 7 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0006 | 0/0 | 3030 | 5 | 1 | 1 | 2 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0007 | 0/0 | 3030 | 5 | 5 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0008 | 1/0 | 3030 | 4 | 2 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0009 | 0/0 | 3030 | 4 | 4 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0010 | 0/0 | 3030 | 4 | 4 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0011 | 0/0 | 3030 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0012 | 0/0 | 3030 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0013 | 0/0 | 3030 | 3 | 0 | 1 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0014 | 0/0 | 3030 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0015 | 0/0 | 3030 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0016 | 0/0 | 3030 | 3 | 2 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0017 | 0/0 | 3030 | 3 | 0 | 3 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0018 | 0/0 | 3030 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0019 | 0/0 | 3030 | 2 | 1 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0020 | 0/0 | 3030 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0021 | 0/0 | 3030 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0022 | 0/0 | 3030 | 2 | 0 | 0 | 0 | 1 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0023 | 0/0 | 3030 | 2 | 0 | 1 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0024 | 0/0 | 3030 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0025 | 0/0 | 3030 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0026 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0027 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0028 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0029 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0030 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0031 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0032 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0033 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0034 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0035 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0036 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0037 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0038 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0039 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0040 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0041 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0042 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0043 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0044 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0045 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0046 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0047 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0048 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0049 | 0/0 | 3030 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0050 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0051 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0052 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0053 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0054 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0055 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0056 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0057 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0058 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0059 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0060 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0061 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0062 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0063 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0064 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0065 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0066 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0067 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0068 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0069 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0070 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
c0071 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2100 | 226 | 15 | 51 | 131 | 7 | 21 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0002 | 0/0 | 2099 | 53 | 23 | 5 | 17 | 2 | 6 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0003 | 0/0 | 2099 | 25 | 19 | 2 | 2 | 0 | 2 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0004 | 0/0 | 2101 | 9 | 0 | 2 | 6 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0005 | 1/0 | 2100 | 5 | 3 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0006 | 0/0 | 2098 | 4 | 4 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0007 | 0/0 | 1497 | 4 | 4 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0008 | 0/0 | 2099 | 4 | 0 | 3 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0009 | 0/0 | 2100 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0010 | 0/0 | 2099 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0011 | 0/0 | 2099 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0012 | 0/0 | 2100 | 2 | 1 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0013 | 0/0 | 2099 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0014 | 0/0 | 2099 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0015 | 0/0 | 1497 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0016 | 0/0 | 2099 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0017 | 0/0 | 2430 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0018 | 0/0 | 2100 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0019 | 0/0 | 2100 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0020 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0021 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0022 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0023 | 0/0 | 2099 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0024 | 0/0 | 2100 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0025 | 0/0 | 2100 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0026 | 0/0 | 2098 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0027 | 0/0 | 2098 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0028 | 0/0 | 2098 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0029 | 0/0 | 2100 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0030 | 0/0 | 2099 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0031 | 0/0 | 2099 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0032 | 0/0 | 2099 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
t0033 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0003 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0004 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0012 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0018 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3030 | 107 | 2 | 22 | 72 | 2 | 9 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0001c0003 | 0/0 | 3030 | 22 | 1 | 0 | 15 | 1 | 5 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0001c0054 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0001c0055 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0001c0061 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0001c0064 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0002 | 0/1 | 3030 | 98 | 11 | 22 | 49 | 3 | 12 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0004 | 0/0 | 3030 | 21 | 11 | 2 | 4 | 2 | 2 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0013 | 0/0 | 3030 | 3 | 0 | 1 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0030 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0031 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0032 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0033 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0003c0007 | 0/0 | 3030 | 5 | 5 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0003c0015 | 0/0 | 3030 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0003c0036 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0003c0041 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0003c0044 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0003c0070 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0004c0005 | 0/0 | 3030 | 9 | 1 | 7 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0005c0010 | 0/0 | 3030 | 4 | 4 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0005c0021 | 0/0 | 3030 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0006c0016 | 0/0 | 3030 | 3 | 2 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0006c0050 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0006c0057 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0007c0006 | 0/0 | 3030 | 5 | 1 | 1 | 2 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0008c0008 | 1/0 | 3030 | 4 | 2 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0008c0038 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0009c0011 | 0/0 | 3030 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0009c0028 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0010c0017 | 0/0 | 3030 | 3 | 0 | 3 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0010c0060 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0011c0009 | 0/0 | 3030 | 4 | 4 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0012c0022 | 0/0 | 3030 | 2 | 0 | 0 | 0 | 1 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0012c0049 | 0/0 | 3030 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0013c0051 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0013c0052 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0013c0053 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0014c0012 | 0/0 | 3030 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0015c0019 | 0/0 | 3030 | 2 | 1 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0015c0035 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0016c0014 | 0/0 | 3030 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0017c0023 | 0/0 | 3030 | 2 | 0 | 1 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0018c0024 | 0/0 | 3030 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0019c0025 | 0/0 | 3030 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0020c0018 | 0/0 | 3030 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0021c0020 | 0/0 | 3030 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0022c0037 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0022c0069 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0023c0027 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0024c0067 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0025c0068 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0026c0066 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0027c0065 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0028c0048 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0029c0059 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0030c0058 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0031c0063 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0032c0071 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0033c0062 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0034c0056 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0035c0029 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0036c0034 | 0/0 | 3030 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0037c0047 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0038c0045 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0039c0046 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0040c0039 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0041c0042 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0042c0043 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0043c0040 | 0/0 | 3030 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0044c0026 | 0/0 | 3030 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5129 | 98 | 2 | 18 | 68 | 2 | 8 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0001c0001t0004 | 0/0 | 5130 | 5 | 0 | 1 | 4 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0001c0001t0012 | 0/0 | 5129 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0001c0001t0018 | 0/0 | 5129 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0001c0001t0019 | 0/0 | 5129 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0001c0001t0023 | 0/0 | 5128 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0001c0003t0002 | 0/0 | 5128 | 20 | 1 | 0 | 13 | 1 | 5 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0001c0003t0003 | 0/0 | 5128 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0001c0054t0002 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0001c0055t0002 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0001c0061t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0001c0064t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0002t0001 | 0/1 | 5129 | 86 | 4 | 21 | 46 | 3 | 11 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0002t0002 | 0/0 | 5128 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0002t0003 | 0/0 | 5128 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0002t0004 | 0/0 | 5130 | 2 | 0 | 0 | 1 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0002t0009 | 0/0 | 5129 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0002t0020 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0002t0024 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0002t0029 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0002t0033 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0004t0002 | 0/0 | 5128 | 9 | 3 | 0 | 4 | 1 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0004t0003 | 0/0 | 5128 | 8 | 7 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0004t0008 | 0/0 | 5128 | 2 | 0 | 1 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0004t0011 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0004t0031 | 0/0 | 5128 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0013t0001 | 0/0 | 5129 | 2 | 0 | 1 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0013t0022 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0030t0013 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0031t0005 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0032t0011 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0002c0033t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0003c0007t0009 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0003c0007t0010 | 0/0 | 5128 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0003c0007t0013 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0003c0015t0002 | 0/0 | 5128 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0003c0036t0002 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0003c0041t0002 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0003c0044t0002 | 0/0 | 5128 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0003c0070t0002 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0004c0005t0001 | 0/0 | 5129 | 9 | 1 | 7 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0005c0010t0003 | 0/0 | 5128 | 4 | 4 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0005c0021t0001 | 0/0 | 5129 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0006c0016t0002 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0006c0016t0003 | 0/0 | 5128 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0006c0016t0006 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0006c0050t0026 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0006c0057t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0007c0006t0001 | 0/0 | 5129 | 5 | 1 | 1 | 2 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0008c0008t0005 | 1/0 | 5129 | 4 | 2 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0008c0038t0012 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0009c0011t0001 | 0/0 | 5129 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0009c0011t0002 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0009c0028t0003 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0010c0017t0002 | 0/0 | 5128 | 3 | 0 | 3 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0010c0060t0001 | 0/0 | 5129 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0011c0009t0002 | 0/0 | 5128 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0011c0009t0016 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0011c0009t0032 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0012c0022t0001 | 0/0 | 5129 | 2 | 0 | 0 | 0 | 1 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0012c0049t0003 | 0/0 | 5128 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0013c0051t0001 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0013c0052t0003 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0013c0053t0014 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0014c0012t0002 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0014c0012t0003 | 0/0 | 5128 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0015c0019t0001 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0015c0019t0002 | 0/0 | 5128 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0015c0035t0003 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0016c0014t0006 | 0/0 | 5127 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0017c0023t0001 | 0/0 | 5129 | 2 | 0 | 1 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0018c0024t0008 | 0/0 | 5128 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0019c0025t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0019c0025t0004 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0020c0018t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0020c0018t0021 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0021c0020t0002 | 0/0 | 5128 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0022c0037t0003 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0022c0069t0003 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0023c0027t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0024c0067t0025 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0025c0068t0001 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0026c0066t0028 | 0/0 | 5127 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0027c0065t0004 | 0/0 | 5130 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0028c0048t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0029c0059t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0030c0058t0007 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0031c0063t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0032c0071t0003 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0033c0062t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0034c0056t0007 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0035c0029t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0036c0034t0001 | 0/0 | 5129 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0037c0047t0027 | 0/0 | 5127 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0038c0045t0002 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0039c0046t0017 | 0/0 | 5459 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0040c0039t0007 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0041c0042t0007 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0042c0043t0030 | 0/0 | 5128 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0043c0040t0015 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
a0044c0026t0001 | 0/0 | 5129 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | copy fasta | chr4 | 6570189 | 6628362 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0004g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0012g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0018g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0019g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0023g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0002 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0054t0002g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0055t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0061t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0064t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0001 | 0/0 | 6 | 0 | 2 | 4 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0003 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0004 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0177 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0003g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0004g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0004g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0009g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0009g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0020g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0024g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0029g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0033g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0003g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0008g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0008g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0011g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0031g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0013t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0013t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0013t0022g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0030t0013g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0031t0005g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0032t0011g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0033t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0003c0007t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0003c0007t0010g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0003c0007t0010g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0003c0007t0013g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0003c0015t0002g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0003c0015t0002g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0003c0015t0002g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0003c0036t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0003c0041t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0003c0044t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0003c0070t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0004c0005t0001g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0004c0005t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0004c0005t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0004c0005t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0004c0005t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0004c0005t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0004c0005t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0005c0010t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0005c0010t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0005c0010t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0005c0021t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0006c0016t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0006c0016t0003g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0006c0016t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0006c0050t0026g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0006c0057t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0007c0006t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0007c0006t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0007c0006t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0007c0006t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0007c0006t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0008c0008t0005g0011 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0008c0008t0005g0012 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0008c0038t0012g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0009c0011t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0009c0011t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0009c0011t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0009c0028t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0010c0017t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0010c0017t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0010c0017t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0010c0060t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0011c0009t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0011c0009t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0011c0009t0016g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0011c0009t0032g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0012c0022t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0012c0022t0001g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0012c0049t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0013c0051t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0013c0052t0003g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0013c0053t0014g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0014c0012t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0014c0012t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0014c0012t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0015c0019t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0015c0019t0002g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0015c0035t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0016c0014t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0016c0014t0006g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0016c0014t0006g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0017c0023t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0017c0023t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0018c0024t0008g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0018c0024t0008g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0019c0025t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0019c0025t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0020c0018t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0020c0018t0021g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0021c0020t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0021c0020t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0022c0037t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0022c0069t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0023c0027t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0024c0067t0025g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0025c0068t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0026c0066t0028g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0027c0065t0004g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0028c0048t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0029c0059t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0030c0058t0007g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0031c0063t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0032c0071t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0033c0062t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0034c0056t0007g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0035c0029t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0036c0034t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0037c0047t0027g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0038c0045t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0039c0046t0017g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0040c0039t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0041c0042t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0042c0043t0030g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0043c0040t0015g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0044c0026t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | GBR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00099 | hp2 | a0002 | c0004 | t0008 | g0192 | EUR | GBR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00140 | hp1 | a0002 | c0004 | t0002 | g0214 | EUR | GBR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00140 | hp2 | a0001 | c0003 | t0002 | g0186 | EUR | GBR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0187 | EUR | FIN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00323 | hp2 | a0012 | c0022 | t0001 | g0247 | EUR | FIN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0329 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0316 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0194 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0274 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0006 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0153 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00639 | hp2 | a0018 | c0024 | t0008 | g0073 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00642 | hp2 | a0010 | c0017 | t0002 | g0226 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00733 | hp1 | a0003 | c0044 | t0002 | g0132 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00738 | hp1 | a0004 | c0005 | t0001 | g0209 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00738 | hp2 | a0018 | c0024 | t0008 | g0081 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01069 | hp1 | a0002 | c0013 | t0001 | g0139 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01070 | hp1 | a0010 | c0017 | t0002 | g0294 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0295 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0019 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01071 | hp2 | a0010 | c0017 | t0002 | g0270 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0257 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0181 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01106 | hp1 | a0017 | c0023 | t0001 | g0246 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0003 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01109 | hp1 | a0026 | c0066 | t0028 | g0131 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0023 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01167 | hp2 | a0008 | c0008 | t0005 | g0011 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01168 | hp2 | a0004 | c0005 | t0001 | g0138 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01169 | hp2 | a0004 | c0005 | t0001 | g0137 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01175 | hp1 | a0002 | c0002 | t0003 | g0245 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01243 | hp1 | a0015 | c0019 | t0002 | g0142 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01255 | hp1 | a0002 | c0004 | t0003 | g0196 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0028 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01256 | hp1 | a0001 | c0001 | t0023 | g0211 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0183 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0217 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0216 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0215 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01358 | hp2 | a0001 | c0001 | t0019 | g0052 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01361 | hp1 | a0001 | c0001 | t0018 | g0284 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01361 | hp2 | a0007 | c0006 | t0001 | g0059 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0330 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0179 | EUR | IBS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0129 | EUR | IBS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01884 | hp1 | a0042 | c0043 | t0030 | g0089 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01884 | hp2 | a0003 | c0041 | t0002 | g0076 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01891 | hp1 | a0013 | c0052 | t0003 | g0225 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01891 | hp2 | a0005 | c0021 | t0001 | g0008 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01928 | hp1 | a0004 | c0005 | t0001 | g0212 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01928 | hp2 | a0027 | c0065 | t0004 | g0148 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0169 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0210 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01943 | hp2 | a0044 | c0026 | t0001 | g0141 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0155 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01952 | hp2 | a0004 | c0005 | t0001 | g0213 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0293 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01978 | hp2 | a0002 | c0004 | t0008 | g0191 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0003 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01993 | hp2 | a0010 | c0060 | t0001 | g0267 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02004 | hp2 | a0004 | c0005 | t0001 | g0005 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0318 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0154 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02055 | hp1 | a0007 | c0006 | t0001 | g0080 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0250 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02056 | hp1 | a0001 | c0003 | t0003 | g0264 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02056 | hp2 | a0001 | c0003 | t0002 | g0320 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0106 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02071 | hp2 | a0007 | c0006 | t0001 | g0159 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0119 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0146 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02129 | hp1 | a0031 | c0063 | t0001 | g0256 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0242 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02132 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02135 | hp1 | a0004 | c0005 | t0001 | g0005 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0287 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02145 | hp1 | a0002 | c0002 | t0029 | g0035 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02145 | hp2 | a0038 | c0045 | t0002 | g0082 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02148 | hp1 | a0004 | c0005 | t0001 | g0005 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0150 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CDX | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02155 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | CDX | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | CDX | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | CDX | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02257 | hp1 | a0021 | c0020 | t0002 | g0049 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02257 | hp2 | a0041 | c0042 | t0007 | g0077 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02258 | hp1 | a0024 | c0067 | t0025 | g0031 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02258 | hp2 | a0003 | c0007 | t0010 | g0042 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02280 | hp1 | a0005 | c0010 | t0003 | g0010 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02280 | hp2 | a0040 | c0039 | t0007 | g0050 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0301 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02451 | hp1 | a0006 | c0050 | t0026 | g0224 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02451 | hp2 | a0015 | c0035 | t0003 | g0166 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0111 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02572 | hp1 | a0001 | c0003 | t0002 | g0202 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02572 | hp2 | a0003 | c0070 | t0002 | g0034 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02602 | hp2 | a0001 | c0003 | t0002 | g0300 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02615 | hp1 | a0005 | c0010 | t0003 | g0043 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02615 | hp2 | a0002 | c0031 | t0005 | g0083 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02622 | hp1 | a0037 | c0047 | t0027 | g0195 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02622 | hp2 | a0002 | c0004 | t0003 | g0207 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02630 | hp1 | a0003 | c0007 | t0013 | g0057 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02630 | hp2 | a0030 | c0058 | t0007 | g0127 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02647 | hp1 | a0002 | c0004 | t0002 | g0208 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02647 | hp2 | a0039 | c0046 | t0017 | g0130 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0018 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02717 | hp1 | a0008 | c0008 | t0005 | g0012 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02717 | hp2 | a0003 | c0015 | t0002 | g0326 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02723 | hp1 | a0013 | c0053 | t0014 | g0040 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02723 | hp2 | a0011 | c0009 | t0002 | g0048 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02809 | hp1 | a0002 | c0004 | t0003 | g0323 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02809 | hp2 | a0002 | c0004 | t0002 | g0188 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02818 | hp1 | a0002 | c0002 | t0002 | g0085 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02818 | hp2 | a0011 | c0009 | t0032 | g0084 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02886 | hp1 | a0006 | c0016 | t0006 | g0125 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02886 | hp2 | a0005 | c0010 | t0003 | g0044 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02895 | hp1 | a0003 | c0015 | t0002 | g0327 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02895 | hp2 | a0001 | c0054 | t0002 | g0220 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02896 | hp1 | a0003 | c0007 | t0010 | g0007 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02896 | hp2 | a0002 | c0004 | t0003 | g0206 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02897 | hp1 | a0003 | c0007 | t0010 | g0007 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02897 | hp2 | a0003 | c0015 | t0002 | g0328 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02965 | hp1 | a0005 | c0010 | t0003 | g0010 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02965 | hp2 | a0001 | c0055 | t0002 | g0122 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02970 | hp1 | a0014 | c0012 | t0003 | g0204 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0004 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02976 | hp1 | a0002 | c0002 | t0009 | g0025 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02976 | hp2 | a0002 | c0004 | t0003 | g0203 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03017 | hp1 | a0012 | c0022 | t0001 | g0315 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0176 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03041 | hp1 | a0003 | c0036 | t0002 | g0036 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03041 | hp2 | a0034 | c0056 | t0007 | g0221 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03130 | hp1 | a0009 | c0011 | t0001 | g0105 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03130 | hp2 | a0016 | c0014 | t0006 | g0201 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03139 | hp1 | a0016 | c0014 | t0006 | g0199 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03139 | hp2 | a0009 | c0011 | t0002 | g0104 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03195 | hp1 | a0002 | c0002 | t0002 | g0325 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03195 | hp2 | a0006 | c0016 | t0002 | g0126 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03209 | hp1 | a0009 | c0028 | t0003 | g0047 | AFR | MSL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03209 | hp2 | a0025 | c0068 | t0001 | g0032 | AFR | MSL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03239 | hp1 | a0002 | c0004 | t0002 | g0161 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0190 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03453 | hp1 | a0021 | c0020 | t0002 | g0045 | AFR | MSL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03453 | hp2 | a0009 | c0011 | t0001 | g0046 | AFR | MSL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03486 | hp1 | a0043 | c0040 | t0015 | g0039 | AFR | MSL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03486 | hp2 | a0002 | c0004 | t0003 | g0078 | AFR | MSL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03490 | hp1 | a0002 | c0002 | t0001 | g0109 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03490 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0143 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03516 | hp1 | a0011 | c0009 | t0002 | g0222 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03516 | hp2 | a0002 | c0002 | t0024 | g0184 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03540 | hp1 | a0014 | c0012 | t0002 | g0197 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03540 | hp2 | a0008 | c0008 | t0005 | g0011 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03579 | hp1 | a0022 | c0037 | t0003 | g0124 | AFR | MSL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03579 | hp2 | a0002 | c0030 | t0013 | g0136 | AFR | MSL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0062 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03669 | hp1 | a0017 | c0023 | t0001 | g0180 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03669 | hp2 | a0001 | c0003 | t0002 | g0054 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03688 | hp1 | a0002 | c0002 | t0004 | g0110 | SAS | STU | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0164 | SAS | STU | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03704 | hp2 | a0012 | c0049 | t0003 | g0098 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03710 | hp2 | a0001 | c0003 | t0002 | g0162 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03831 | hp1 | a0001 | c0001 | t0012 | g0030 | SAS | BEB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03831 | hp2 | a0006 | c0016 | t0003 | g0271 | SAS | BEB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | BEB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0003 | SAS | BEB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG04184 | hp2 | a0001 | c0003 | t0002 | g0027 | SAS | BEB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG04204 | hp1 | a0001 | c0003 | t0002 | g0070 | SAS | STU | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0178 | SAS | STU | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18522 | hp1 | a0002 | c0004 | t0003 | g0055 | AFR | YRI | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18522 | hp2 | a0002 | c0004 | t0011 | g0038 | AFR | YRI | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18612 | hp1 | a0001 | c0003 | t0002 | g0094 | EAS | CHB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0051 | EAS | CHB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | CHB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | CHB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18906 | hp1 | a0011 | c0009 | t0016 | g0026 | AFR | YRI | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18906 | hp2 | a0002 | c0002 | t0002 | g0123 | AFR | YRI | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18940 | hp1 | a0002 | c0013 | t0022 | g0016 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18941 | hp2 | a0028 | c0048 | t0001 | g0120 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18942 | hp1 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18944 | hp2 | a0020 | c0018 | t0001 | g0020 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18948 | hp1 | a0002 | c0002 | t0020 | g0017 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18949 | hp1 | a0001 | c0001 | t0004 | g0281 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18949 | hp2 | a0002 | c0002 | t0004 | g0006 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18950 | hp2 | a0001 | c0003 | t0002 | g0265 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18952 | hp1 | a0001 | c0003 | t0003 | g0228 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0332 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0144 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18953 | hp2 | a0033 | c0062 | t0001 | g0102 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0289 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18956 | hp1 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0171 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18963 | hp1 | a0019 | c0025 | t0001 | g0189 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18963 | hp2 | a0002 | c0004 | t0002 | g0218 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18965 | hp2 | a0019 | c0025 | t0004 | g0168 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18966 | hp1 | a0002 | c0002 | t0033 | g0158 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18966 | hp2 | a0001 | c0064 | t0001 | g0243 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18967 | hp2 | a0002 | c0033 | t0001 | g0145 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18970 | hp2 | a0001 | c0003 | t0002 | g0233 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18971 | hp1 | a0020 | c0018 | t0021 | g0020 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18971 | hp2 | a0002 | c0004 | t0002 | g0170 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0227 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18977 | hp1 | a0029 | c0059 | t0001 | g0304 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0310 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18980 | hp1 | a0001 | c0061 | t0001 | g0067 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0278 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18982 | hp2 | a0001 | c0003 | t0002 | g0066 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18983 | hp2 | a0001 | c0003 | t0002 | g0061 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18990 | hp2 | a0007 | c0006 | t0001 | g0156 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18991 | hp2 | a0001 | c0003 | t0002 | g0071 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18994 | hp1 | a0002 | c0004 | t0002 | g0112 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18994 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18997 | hp2 | a0001 | c0003 | t0002 | g0072 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0151 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19005 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19007 | hp2 | a0001 | c0003 | t0002 | g0291 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0319 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0118 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19012 | hp1 | a0036 | c0034 | t0001 | g0157 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19030 | hp1 | a0015 | c0019 | t0001 | g0100 | AFR | LWK | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19030 | hp2 | a0005 | c0021 | t0001 | g0008 | AFR | LWK | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19043 | hp1 | a0032 | c0071 | t0003 | g0333 | AFR | LWK | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19043 | hp2 | a0016 | c0014 | t0006 | g0200 | AFR | LWK | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19060 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19063 | hp1 | a0001 | c0003 | t0002 | g0058 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0182 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0175 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19074 | hp2 | a0035 | c0029 | t0001 | g0140 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0331 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0014 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0152 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19081 | hp1 | a0006 | c0057 | t0001 | g0279 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0174 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19085 | hp1 | a0002 | c0004 | t0002 | g0219 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19090 | hp1 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0173 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19091 | hp1 | a0002 | c0013 | t0001 | g0016 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA20129 | hp1 | a0022 | c0069 | t0003 | g0033 | AFR | ASW | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ASW | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0172 | EUR | TSI | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA20752 | hp2 | a0007 | c0006 | t0001 | g0185 | EUR | TSI | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | GIH | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA20905 | hp2 | a0002 | c0004 | t0031 | g0260 | SAS | GIH | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02109 | hp2 | a0014 | c0012 | t0003 | g0205 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0087 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02486 | hp2 | a0002 | c0004 | t0003 | g0056 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02559 | hp1 | a0002 | c0004 | t0002 | g0198 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02559 | hp2 | a0003 | c0007 | t0009 | g0041 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0163 | AFR | MSL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03471 | hp2 | a0013 | c0051 | t0001 | g0223 | AFR | MSL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG06807 | hp1 | a0004 | c0005 | t0001 | g0018 | AFR | USA | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG06807 | hp2 | a0002 | c0002 | t0009 | g0037 | AFR | USA | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18955 | hp2 | a0023 | c0027 | t0001 | g0121 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA20300 | hp1 | a0008 | c0038 | t0012 | g0053 | AFR | USA | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA20300 | hp2 | a0002 | c0032 | t0011 | g0024 | AFR | USA | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0177 | REF | REF | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
homoSapiens_grch38 | hp1 | a0008 | c0008 | t0005 | g0012 | REF | REF | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:6575322
|
G | A | 1 | a0044 | 1 | HG01943.hp2 | missense_variant | MODERATE | c.112G>A | p.Asp38Asn | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/19 | 134/5129 | 112/3030 | 38/1009 | chr4 | 6575322 | ||
chr4:6576651
|
G | A | 1 | a0023 | 1 | NA18955.hp2 | missense_variant | MODERATE | c.212G>A | p.Arg71Gln | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/19 | 234/5129 | 212/3030 | 71/1009 | chr4 | 6576651 | ||
chr4:6578397
|
G | A | 1 | a0009 | 4 | HG03130.hp1 HG03139.hp2 HG03209.hp1 others(1): Show |
missense_variant | MODERATE | c.290G>A | p.Arg97His | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/19 | 312/5129 | 290/3030 | 97/1009 | chr4 | 6578397 | ||
chr4:6589108
|
A | T | 3 | a0024a0025a0026 | 3 | HG01109.hp1 HG02258.hp1 HG03209.hp2 |
missense_variant | MODERATE | c.628A>T | p.Ile210Phe | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/19 | 650/5129 | 628/3030 | 210/1009 | chr4 | 6589108 | ||
chr4:6593220
|
A | C | 18 | a0001a0006a0010others(15): Show | 164 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(161): Show |
missense_variant | MODERATE | c.728A>C | p.Gln243Pro | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 6/19 | 750/5129 | 728/3030 | 243/1009 | chr4 | 6593220 | ||
chr4:6593273
|
C | T | 1 | a0027 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.781C>T | p.Leu261Phe | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 6/19 | 803/5129 | 781/3030 | 261/1009 | chr4 | 6593273 | ||
chr4:6594633
|
G | A | 14 | a0002a0004a0007others(11): Show | 161 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(158): Show |
missense_variant | MODERATE | c.958G>A | p.Val320Met | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/19 | 980/5129 | 958/3030 | 320/1009 | chr4 | 6594633 | ||
chr4:6594658
|
A | G | 1 | a0037 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.983A>G | p.Tyr328Cys | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/19 | 1005/5129 | 983/3030 | 328/1009 | chr4 | 6594658 | ||
chr4:6597148
|
C | T | 3 | a0005a0038a0039 | 8 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
missense_variant | MODERATE | c.1093C>T | p.Arg365Cys | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 8/19 | 1115/5129 | 1093/3030 | 365/1009 | chr4 | 6597148 | ||
chr4:6598285
|
A | G | 23 | a0001a0003a0005others(20): Show | 187 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(184): Show |
missense_variant | MODERATE | c.1336A>G | p.Met446Val | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/19 | 1358/5129 | 1336/3030 | 446/1009 | chr4 | 6598285 | ||
chr4:6605118
|
C | G | 1 | a0019 | 2 | NA18963.hp1 NA18965.hp2 |
missense_variant | MODERATE | c.1603C>G | p.Leu535Val | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/19 | 1625/5129 | 1603/3030 | 535/1009 | chr4 | 6605118 | ||
chr4:6605137
|
A | G | 24 | a0001a0003a0005others(21): Show | 191 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(188): Show |
missense_variant | MODERATE | c.1622A>G | p.Asn541Ser | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/19 | 1644/5129 | 1622/3030 | 541/1009 | chr4 | 6605137 | ||
chr4:6605230
|
G | A | 1 | a0035 | 1 | NA19074.hp2 | missense_variant | MODERATE | c.1715G>A | p.Arg572His | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/19 | 1737/5129 | 1715/3030 | 572/1009 | chr4 | 6605230 | ||
chr4:6605319
|
A | G | 1 | a0018 | 2 | HG00639.hp2 HG00738.hp2 |
missense_variant | MODERATE | c.1804A>G | p.Ile602Val | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/19 | 1826/5129 | 1804/3030 | 602/1009 | chr4 | 6605319 | ||
chr4:6609162
|
G | A | 1 | a0010 | 4 | HG00642.hp2 HG01070.hp1 HG01071.hp2 others(1): Show |
missense_variant | MODERATE | c.1870G>A | p.Gly624Arg | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 12/19 | 1892/5129 | 1870/3030 | 624/1009 | chr4 | 6609162 | ||
chr4:6609208
|
C | T | 1 | a0036 | 1 | NA19012.hp1 | missense_variant | MODERATE | c.1916C>T | p.Pro639Leu | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 12/19 | 1938/5129 | 1916/3030 | 639/1009 | chr4 | 6609208 | ||
chr4:6609803
|
T | C | 3 | a0011a0014a0037 | 8 | HG02109.hp2 HG02622.hp1 HG02723.hp2 others(5): Show |
missense_variant | MODERATE | c.2012T>C | p.Met671Thr | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 13/19 | 2034/5129 | 2012/3030 | 671/1009 | chr4 | 6609803 | ||
chr4:6609817
|
T | C | 3 | a0011a0014a0037 | 8 | HG02109.hp2 HG02622.hp1 HG02723.hp2 others(5): Show |
missense_variant | MODERATE | c.2026T>C | p.Tyr676His | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 13/19 | 2048/5129 | 2026/3030 | 676/1009 | chr4 | 6609817 | ||
chr4:6609833
|
G | A | 3 | a0013a0026a0042 | 5 | HG01109.hp1 HG01884.hp1 HG01891.hp1 others(2): Show |
missense_variant | MODERATE | c.2042G>A | p.Arg681His | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 13/19 | 2064/5129 | 2042/3030 | 681/1009 | chr4 | 6609833 | ||
chr4:6609887
|
G | A | 1 | a0029 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.2096G>A | p.Arg699Gln | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 13/19 | 2118/5129 | 2096/3030 | 699/1009 | chr4 | 6609887 | ||
chr4:6610949
|
C | T | 1 | a0020 | 2 | NA18944.hp2 NA18971.hp1 |
missense_variant | MODERATE | c.2329C>T | p.Arg777Trp | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 14/19 | 2351/5129 | 2329/3030 | 777/1009 | chr4 | 6610949 | ||
chr4:6610983
|
A | G | 1 | a0034 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.2363A>G | p.Gln788Arg | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 14/19 | 2385/5129 | 2363/3030 | 788/1009 | chr4 | 6610983 | ||
chr4:6611237
|
C | T | 1 | a0015 | 3 | HG01243.hp1 HG02451.hp2 NA19030.hp1 |
missense_variant | MODERATE | c.2522C>T | p.Ala841Val | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/19 | 2544/5129 | 2522/3030 | 841/1009 | chr4 | 6611237 | ||
chr4:6611254
|
G | A | 1 | a0039 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.2539G>A | p.Val847Met | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/19 | 2561/5129 | 2539/3030 | 847/1009 | chr4 | 6611254 | ||
chr4:6614302
|
C | T | 1 | a0031 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.2648C>T | p.Pro883Leu | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/19 | 2670/5129 | 2648/3030 | 883/1009 | chr4 | 6614302 | ||
chr4:6614329
|
C | T | 3 | a0004a0022a0032 | 12 | HG00738.hp1 HG01168.hp2 HG01169.hp2 others(9): Show |
missense_variant | MODERATE | c.2675C>T | p.Thr892Met | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/19 | 2697/5129 | 2675/3030 | 892/1009 | chr4 | 6614329 | ||
chr4:6619995
|
G | T | 5 | a0030a0034a0040others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02630.hp2 others(2): Show |
missense_variant | MODERATE | c.2883G>T | p.Leu961Phe | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/19 | 2905/5129 | 2883/3030 | 961/1009 | chr4 | 6619995 | ||
chr4:6621257
|
C | T | 1 | a0033 | 1 | NA18953.hp2 | missense_variant | MODERATE | c.3002C>T | p.Thr1001Met | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 3024/5129 | 3002/3030 | 1001/1009 | chr4 | 6621257 | ||
chr4:6622759
|
GTAAGATG others(1745): Show |
G | 5 | a0030a0034a0040others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02630.hp2 others(2): Show |
splice_region_variant | LOW | c.*1475_*3226del | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | chr4 | 6622759 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:6575324
|
C | T | 3 | a0003c0070a0022c0069a0032c0071 | 3 | HG02572.hp2 NA19043.hp1 NA20129.hp1 |
synonymous_variant | LOW | c.114C>T | p.Asp38Asp | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/19 | 136/5129 | 114/3030 | 38/1009 | chr4 | 6575324 | ||
chr4:6597249
|
G | A | 7 | a0003c0036a0005c0010a0005c0021others(4): Show | 11 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(8): Show |
synonymous_variant | LOW | c.1194G>A | p.Leu398Leu | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 8/19 | 1216/5129 | 1194/3030 | 398/1009 | chr4 | 6597249 | ||
chr4:6600651
|
G | A | 14 | a0001c0054a0001c0055a0003c0015others(11): Show | 19 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
synonymous_variant | LOW | c.1434G>A | p.Ser478Ser | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/19 | 1456/5129 | 1434/3030 | 478/1009 | chr4 | 6600651 | ||
chr4:6600687
|
C | T | 1 | a0001c0064 | 1 | NA18966.hp2 | synonymous_variant | LOW | c.1470C>T | p.Ile490Ile | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/19 | 1492/5129 | 1470/3030 | 490/1009 | chr4 | 6600687 | ||
chr4:6605195
|
G | A | 1 | a0003c0007 | 5 | HG02258.hp2 HG02559.hp2 HG02630.hp1 others(2): Show |
synonymous_variant | LOW | c.1680G>A | p.Ala560Ala | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/19 | 1702/5129 | 1680/3030 | 560/1009 | chr4 | 6605195 | ||
chr4:6605243
|
G | A | 1 | a0040c0039 | 1 | HG02280.hp2 | synonymous_variant | LOW | c.1728G>A | p.Ala576Ala | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/19 | 1750/5129 | 1728/3030 | 576/1009 | chr4 | 6605243 | ||
chr4:6605270
|
C | T | 2 | a0002c0013a0029c0059 | 4 | HG01069.hp1 NA18940.hp1 NA18977.hp1 others(1): Show |
synonymous_variant | LOW | c.1755C>T | p.Asn585Asn | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/19 | 1777/5129 | 1755/3030 | 585/1009 | chr4 | 6605270 | ||
chr4:6609230
|
G | A | 2 | a0002c0030a0024c0067 | 2 | HG02258.hp1 HG03579.hp2 |
synonymous_variant | LOW | c.1938G>A | p.Ala646Ala | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 12/19 | 1960/5129 | 1938/3030 | 646/1009 | chr4 | 6609230 | ||
chr4:6609906
|
A | G | 1 | a0002c0033 | 1 | NA18967.hp2 | synonymous_variant | LOW | c.2115A>G | p.Gln705Gln | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 13/19 | 2137/5129 | 2115/3030 | 705/1009 | chr4 | 6609906 | ||
chr4:6614228
|
G | A | 1 | a0001c0061 | 1 | NA18980.hp1 | synonymous_variant | LOW | c.2574G>A | p.Pro858Pro | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/19 | 2596/5129 | 2574/3030 | 858/1009 | chr4 | 6614228 | ||
chr4:6617405
|
C | T | 2 | a0003c0041a0013c0053 | 2 | HG01884.hp2 HG02723.hp1 |
synonymous_variant | LOW | c.2727C>T | p.Asp909Asp | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/19 | 2749/5129 | 2727/3030 | 909/1009 | chr4 | 6617405 | ||
chr4:6617438
|
A | G | 68 | a0001c0001a0001c0003a0001c0054others(65): Show | 356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
synonymous_variant | LOW | c.2760A>G | p.Leu920Leu | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/19 | 2782/5129 | 2760/3030 | 920/1009 | chr4 | 6617438 | ||
chr4:6617477
|
G | A | 31 | a0001c0001a0001c0054a0001c0061others(28): Show | 258 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(255): Show |
synonymous_variant | LOW | c.2799G>A | p.Val933Val | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/19 | 2821/5129 | 2799/3030 | 933/1009 | chr4 | 6617477 | ||
chr4:6619935
|
G | T | 1 | a0002c0032 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.2823G>T | p.Leu941Leu | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/19 | 2845/5129 | 2823/3030 | 941/1009 | chr4 | 6619935 | ||
chr4:6619950
|
C | G | 1 | a0026c0066 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.2838C>G | p.Ser946Ser | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/19 | 2860/5129 | 2838/3030 | 946/1009 | chr4 | 6619950 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:6575196
|
C | G | 1 | a0002c0002t0033 | 1 | NA18966.hp1 | 5_prime_UTR_variant | MODIFIER | c.-15C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/19 | 15 | chr4 | 6575196 | |||||
chr4:6575201
|
T | G | 8 | a0002c0002t0009a0002c0004t0011a0002c0032t0011others(5): Show | 11 | HG02258.hp2 HG02559.hp2 HG02723.hp1 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-10T>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/19 | 10 | chr4 | 6575201 | |||||
chr4:6621305
|
G | T | 90 | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(87): Show | 346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
3_prime_UTR_variant | MODIFIER | c.*20G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 20 | chr4 | 6621305 | |||||
chr4:6621476
|
A | G | 3 | a0002c0030t0013a0003c0007t0010a0003c0007t0013 | 5 | HG02258.hp2 HG02630.hp1 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*191A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 191 | chr4 | 6621476 | |||||
chr4:6621490
|
C | G | 5 | a0030c0058t0007a0034c0056t0007a0040c0039t0007others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*205C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 205 | chr4 | 6621490 | |||||
chr4:6621514
|
C | G | 2 | a0011c0009t0016a0011c0009t0032 | 2 | HG02818.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*229C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 229 | chr4 | 6621514 | |||||
chr4:6621557
|
G | A | 2 | a0006c0016t0006a0016c0014t0006 | 4 | HG02886.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*272G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 272 | chr4 | 6621557 | |||||
chr4:6621605
|
G | A | 43 | a0001c0001t0001a0001c0001t0004a0001c0001t0018others(40): Show | 248 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(245): Show |
3_prime_UTR_variant | MODIFIER | c.*320G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 320 | chr4 | 6621605 | |||||
chr4:6621615
|
C | T | 2 | a0002c0004t0008a0018c0024t0008 | 4 | HG00099.hp2 HG00639.hp2 HG00738.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*330C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 330 | chr4 | 6621615 | |||||
chr4:6621737
|
C | A | 1 | a0006c0050t0026 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*452C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 452 | chr4 | 6621737 | |||||
chr4:6621744
|
G | A | 1 | a0001c0001t0018 | 1 | HG01361.hp1 | 3_prime_UTR_variant | MODIFIER | c.*459G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 459 | chr4 | 6621744 | |||||
chr4:6621779
|
T | C | 1 | a0001c0001t0019 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*494T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 494 | chr4 | 6621779 | |||||
chr4:6621785
|
G | A | 1 | a0002c0002t0020 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*500G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 500 | chr4 | 6621785 | |||||
chr4:6621821
|
G | A | 1 | a0037c0047t0027 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*536G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 536 | chr4 | 6621821 | |||||
chr4:6621892
|
A | G | 1 | a0002c0004t0031 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*607A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 607 | chr4 | 6621892 | |||||
chr4:6622000
|
G | A | 1 | a0020c0018t0021 | 1 | NA18971.hp1 | 3_prime_UTR_variant | MODIFIER | c.*715G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 715 | chr4 | 6622000 | |||||
chr4:6622174
|
G | A | 5 | a0030c0058t0007a0034c0056t0007a0040c0039t0007others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*889G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 889 | chr4 | 6622174 | |||||
chr4:6622287
|
G | A | 1 | a0002c0013t0022 | 1 | NA18940.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1002G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 1002 | chr4 | 6622287 | |||||
chr4:6622439
|
C | CT | 40 | a0001c0001t0001a0001c0001t0012a0001c0001t0018others(37): Show | 240 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(237): Show |
3_prime_UTR_variant | MODIFIER | c.*1168dupT | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 1169 | INFO_REALIGN_3_PRIME | chr4 | 6622439 | ||||
chr4:6622439
|
C | CTT | 4 | a0001c0001t0004a0002c0002t0004a0019c0025t0004others(1): Show | 9 | HG01928.hp2 HG01978.hp1 HG03688.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1167_*1168dupTT | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 1169 | INFO_REALIGN_3_PRIME | chr4 | 6622439 | ||||
chr4:6622677
|
C | G | 1 | a0042c0043t0030 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1392C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 1392 | chr4 | 6622677 | |||||
chr4:6622746
|
T | TAAAGAGT others(323): Show |
1 | a0039c0046t0017 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1475_*1476insGGCC others(326): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 1476 | INFO_REALIGN_3_PRIME | chr4 | 6622746 | ||||
chr4:6622898
|
G | A | 1 | a0002c0002t0024 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1613G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 1613 | chr4 | 6622898 | |||||
chr4:6622946
|
T | G | 2 | a0006c0016t0006a0016c0014t0006 | 4 | HG02886.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1661T>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 1661 | chr4 | 6622946 | |||||
chr4:6623044
|
A | G | 94 | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(91): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
3_prime_UTR_variant | MODIFIER | c.*1759A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 1759 | chr4 | 6623044 | |||||
chr4:6623069
|
C | T | 1 | a0024c0067t0025 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1784C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 1784 | chr4 | 6623069 | |||||
chr4:6623211
|
G | A | 16 | a0001c0003t0003a0002c0002t0003a0002c0004t0003others(13): Show | 30 | HG01175.hp1 HG01255.hp1 HG01891.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1926G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 1926 | chr4 | 6623211 | |||||
chr4:6623298
|
C | T | 1 | a0039c0046t0017 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2013C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 2013 | chr4 | 6623298 | |||||
chr4:6623339
|
T | A | 1 | a0002c0004t0031 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2054T>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 2054 | chr4 | 6623339 | |||||
chr4:6623346
|
CA | C | 88 | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(85): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
3_prime_UTR_variant | MODIFIER | c.*2055delA | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 2055 | INFO_REALIGN_3_PRIME | chr4 | 6623346 | ||||
chr4:6623346
|
CAA | C | 5 | a0006c0016t0006a0006c0050t0026a0016c0014t0006others(2): Show | 7 | HG01109.hp1 HG02451.hp1 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2054_*2055delAA | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 2054 | INFO_REALIGN_3_PRIME | chr4 | 6623346 | ||||
chr4:6623352
|
A | C | 87 | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(84): Show | 343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
3_prime_UTR_variant | MODIFIER | c.*2067A>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 2067 | chr4 | 6623352 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:6575352
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG03704.hp1 | splice_region_variant&intron_variant | LOW | c.138+4G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/18 | chr4 | 6575352 | ||||||
chr4:6575399
|
C | G | 1 | a0032c0071t0003g0333 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.138+51C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/18 | chr4 | 6575399 | ||||||
chr4:6575466
|
T | G | 1 | a0001c0001t0001g0022 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.138+118T>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/18 | chr4 | 6575466 | ||||||
chr4:6575596
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.138+248G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/18 | chr4 | 6575596 | ||||||
chr4:6575597
|
A | G | 1 | a0001c0001t0001g0022 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.138+249A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/18 | chr4 | 6575597 | ||||||
chr4:6575599
|
G | A | 1 | a0002c0002t0001g0023 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.138+251G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/18 | chr4 | 6575599 | ||||||
chr4:6575604
|
T | G | 1 | a0001c0001t0001g0022 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.138+256T>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/18 | chr4 | 6575604 | ||||||
chr4:6575616
|
G | A | 3 | a0002c0002t0009g0025a0002c0032t0011g0024a0011c0009t0016g0026 | 3 | HG02976.hp1 NA18906.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.138+268G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/18 | chr4 | 6575616 | ||||||
chr4:6575642
|
T | G | 1 | a0001c0003t0002g0027 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.138+294T>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/18 | chr4 | 6575642 | ||||||
chr4:6575719
|
C | T | 4 | a0001c0001t0001g0331a0002c0002t0001g0332a0020c0018t0001g0020others(1): Show | 4 | NA18944.hp2 NA18952.hp2 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.138+371C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/18 | chr4 | 6575719 | ||||||
chr4:6575722
|
C | T | 1 | a0001c0001t0001g0330 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.138+374C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/18 | chr4 | 6575722 | ||||||
chr4:6575729
|
G | A | 2 | a0002c0002t0001g0028a0002c0002t0001g0029 | 2 | HG00735.hp2 HG01255.hp2 |
intron_variant | MODIFIER | c.138+381G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/18 | chr4 | 6575729 | ||||||
chr4:6575913
|
G | C | 1 | a0001c0001t0012g0030 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.138+565G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/18 | chr4 | 6575913 | ||||||
chr4:6575983
|
C | A | 2 | a0024c0067t0025g0031a0025c0068t0001g0032 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.139-595C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/18 | chr4 | 6575983 | ||||||
chr4:6576047
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.139-531C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/18 | chr4 | 6576047 | ||||||
chr4:6576161
|
T | C | 14 | a0002c0002t0009g0025a0002c0002t0009g0037a0002c0002t0029g0035others(11): Show | 15 | HG02145.hp1 HG02258.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.139-417T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/18 | chr4 | 6576161 | ||||||
chr4:6576265
|
C | T | 3 | a0003c0007t0009g0041a0003c0007t0010g0007a0003c0007t0010g0042 | 4 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.139-313C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/18 | chr4 | 6576265 | ||||||
chr4:6576325
|
G | A | 9 | a0005c0010t0003g0043a0005c0010t0003g0044a0005c0021t0001g0008others(6): Show | 10 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.139-253G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/18 | chr4 | 6576325 | ||||||
chr4:6576357
|
G | T | 5 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(2): Show | 5 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-221G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/18 | chr4 | 6576357 | ||||||
chr4:6576380
|
C | T | 1 | a0002c0002t0001g0029 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.139-198C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/18 | chr4 | 6576380 | ||||||
chr4:6576444
|
G | A | 1 | a0002c0002t0001g0051 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.139-134G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 1/18 | chr4 | 6576444 | ||||||
chr4:6576760
|
A | G | 280 | a0001c0001t0001g0021a0001c0001t0001g0107a0001c0001t0001g0115others(277): Show | 298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): Show |
intron_variant | MODIFIER | c.285+36A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/18 | chr4 | 6576760 | ||||||
chr4:6576887
|
C | T | 6 | a0002c0002t0002g0325a0003c0015t0002g0326a0003c0015t0002g0327others(3): Show | 6 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+163C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/18 | chr4 | 6576887 | ||||||
chr4:6576973
|
C | T | 1 | a0001c0001t0001g0324 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.285+249C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/18 | chr4 | 6576973 | ||||||
chr4:6577094
|
G | C | 1 | a0001c0001t0001g0022 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.285+370G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/18 | chr4 | 6577094 | ||||||
chr4:6577111
|
C | T | 1 | a0002c0002t0001g0023 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.285+387C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/18 | chr4 | 6577111 | ||||||
chr4:6577125
|
C | T | 1 | a0002c0004t0003g0323 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.285+401C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/18 | chr4 | 6577125 | ||||||
chr4:6577180
|
G | A | 11 | a0005c0010t0003g0043a0005c0010t0003g0044a0005c0021t0001g0008others(8): Show | 12 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.285+456G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/18 | chr4 | 6577180 | ||||||
chr4:6577188
|
C | T | 4 | a0002c0002t0009g0037a0002c0004t0011g0038a0013c0053t0014g0040others(1): Show | 4 | HG02723.hp1 HG03486.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+464C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/18 | chr4 | 6577188 | ||||||
chr4:6577206
|
C | G | 6 | a0002c0002t0002g0325a0003c0015t0002g0326a0003c0015t0002g0327others(3): Show | 6 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+482C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/18 | chr4 | 6577206 | ||||||
chr4:6577277
|
A | G | 3 | a0003c0007t0009g0041a0003c0007t0010g0007a0003c0007t0010g0042 | 4 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+553A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/18 | chr4 | 6577277 | ||||||
chr4:6577356
|
C | T | 104 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(101): Show | 106 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.285+632C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/18 | chr4 | 6577356 | ||||||
chr4:6577378
|
A | C | 6 | a0002c0002t0002g0325a0003c0015t0002g0326a0003c0015t0002g0327others(3): Show | 6 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+654A>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/18 | chr4 | 6577378 | ||||||
chr4:6577412
|
A | G | 5 | a0001c0054t0002g0220a0006c0050t0026g0224a0011c0009t0002g0222others(2): Show | 5 | HG02451.hp1 HG02895.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+688A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/18 | chr4 | 6577412 | ||||||
chr4:6577485
|
C | A | 1 | a0001c0001t0001g0022 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.285+761C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/18 | chr4 | 6577485 | ||||||
chr4:6577499
|
C | T | 2 | a0013c0053t0014g0040a0043c0040t0015g0039 | 2 | HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.285+775C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/18 | chr4 | 6577499 | ||||||
chr4:6577664
|
G | A | 1 | a0001c0001t0019g0052 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.286-729G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/18 | chr4 | 6577664 | ||||||
chr4:6577687
|
G | C | 1 | a0008c0038t0012g0053 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.286-706G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/18 | chr4 | 6577687 | ||||||
chr4:6577693
|
G | A | 1 | a0001c0003t0002g0054 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.286-700G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/18 | chr4 | 6577693 | ||||||
chr4:6577874
|
T | G | 3 | a0002c0002t0009g0037a0013c0053t0014g0040a0043c0040t0015g0039 | 3 | HG02723.hp1 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.286-519T>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/18 | chr4 | 6577874 | ||||||
chr4:6578362
|
G | A | 5 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(2): Show | 5 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-31G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/18 | chr4 | 6578362 | ||||||
chr4:6578556
|
A | G | 113 | a0001c0001t0001g0103a0001c0001t0001g0229a0001c0001t0001g0230others(110): Show | 116 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.391+58A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6578556 | ||||||
chr4:6578780
|
C | G | 5 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(2): Show | 5 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.391+282C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6578780 | ||||||
chr4:6578816
|
C | T | 1 | a0033c0062t0001g0102 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.391+318C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6578816 | ||||||
chr4:6578964
|
T | TCACCAC | 19 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0117others(16): Show | 21 | HG00423.hp2 HG02071.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.391+476_391+481dup others(6): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6578964 | |||||
chr4:6578970
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.391+472C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6578970 | ||||||
chr4:6578986
|
C | G | 1 | a0001c0001t0001g0321 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.391+488C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6578986 | ||||||
chr4:6578998
|
T | TACCATCA others(296): Show |
3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG00099.hp1 HG01433.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.391+588_391+589ins others(303): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6578998 | |||||
chr4:6579009
|
CCACCACC others(83): Show |
C | 20 | a0001c0001t0001g0079a0001c0001t0001g0129a0001c0003t0002g0058others(17): Show | 22 | HG00738.hp2 HG01517.hp2 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.391+544_391+633del others(90): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579009 | |||||
chr4:6579009
|
CCACCACC others(125): Show |
C | 2 | a0002c0004t0003g0055a0002c0004t0003g0056 | 2 | HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.391+536_391+667del | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579009 | |||||
chr4:6579015
|
CCACCAT | C | 3 | a0001c0054t0002g0220a0011c0009t0002g0222a0034c0056t0007g0221 | 3 | HG02895.hp2 HG03041.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.391+529_391+534del others(6): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579015 | |||||
chr4:6579021
|
T | C | 4 | a0001c0055t0002g0122a0002c0002t0009g0037a0024c0067t0025g0031others(1): Show | 4 | HG02258.hp1 HG02965.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+523T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579021 | ||||||
chr4:6579039
|
CCAT | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 4 | HG00621.hp1 NA18612.hp1 NA19067.hp1 others(1): Show |
intron_variant | MODIFIER | c.391+544_391+546del others(3): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579039 | |||||
chr4:6579042
|
T | C | 69 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(66): Show | 72 | HG00609.hp2 HG00639.hp2 HG00733.hp1 others(69): Show |
intron_variant | MODIFIER | c.391+544T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579042 | ||||||
chr4:6579042
|
T | TCACCACC others(551): Show |
1 | a0002c0002t0004g0110 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.391+576_391+577ins others(558): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579042 | |||||
chr4:6579042
|
T | TCACCACC others(1288): Show |
1 | a0002c0002t0001g0109 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.391+576_391+577ins others(1295): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579042 | |||||
chr4:6579045
|
C | CCACCATC others(551): Show |
1 | a0002c0002t0001g0106 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.391+576_391+577ins others(558): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579045 | |||||
chr4:6579045
|
C | CCACCATC others(1001): Show |
1 | a0001c0001t0001g0107 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.391+576_391+577ins others(1008): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579045 | |||||
chr4:6579045
|
C | CCACCATC others(467): Show |
1 | a0002c0002t0001g0108 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.391+576_391+577ins others(474): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579045 | |||||
chr4:6579045
|
C | CCACCATC others(551): Show |
7 | a0001c0001t0001g0115a0002c0002t0001g0013a0002c0002t0001g0051others(4): Show | 8 | HG02523.hp2 HG02602.hp1 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.391+576_391+577ins others(558): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579045 | |||||
chr4:6579045
|
C | CCACCATC others(542): Show |
2 | a0002c0002t0001g0014a0002c0002t0001g0116 | 3 | NA18962.hp2 NA19064.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.391+576_391+577ins others(549): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579045 | |||||
chr4:6579045
|
C | CCACCATC others(986): Show |
1 | a0001c0001t0001g0117 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.391+576_391+577ins others(993): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579045 | |||||
chr4:6579045
|
C | CCACCATC others(548): Show |
1 | a0002c0002t0001g0119 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.391+576_391+577ins others(555): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579045 | |||||
chr4:6579045
|
C | CCACCATC others(581): Show |
1 | a0002c0002t0001g0118 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.391+576_391+577ins others(588): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579045 | |||||
chr4:6579045
|
C | CCACCATC others(563): Show |
1 | a0028c0048t0001g0120 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.391+576_391+577ins others(570): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579045 | |||||
chr4:6579051
|
T | C | 1 | a0010c0017t0002g0226 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.391+553T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579051 | ||||||
chr4:6579051
|
T | TCACCACC others(38): Show |
2 | a0002c0004t0002g0218a0002c0004t0002g0219 | 2 | NA18963.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.391+588_391+589ins others(45): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579051 | |||||
chr4:6579061
|
C | A | 1 | a0002c0002t0001g0227 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.391+563C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579061 | ||||||
chr4:6579063
|
T | C | 1 | a0001c0003t0003g0228 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.391+565T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579063 | ||||||
chr4:6579063
|
T | TCACCATC others(512): Show |
1 | a0023c0027t0001g0121 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.391+576_391+577ins others(519): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579063 | |||||
chr4:6579066
|
C | CCACCACC others(515): Show |
1 | a0001c0003t0002g0027 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.391+570_391+571ins others(522): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579066 | |||||
chr4:6579069
|
T | C | 1 | a0001c0003t0002g0027 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.391+571T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579069 | ||||||
chr4:6579069
|
T | TCAC | 60 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(57): Show | 63 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.391+586_391+588dup others(3): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579069 | |||||
chr4:6579069
|
T | TCACCACC others(38): Show |
2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | NA18999.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.391+588_391+589ins others(45): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579069 | |||||
chr4:6579069
|
T | TCACCAGC others(448): Show |
1 | a0026c0066t0028g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.391+576_391+577ins others(455): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579069 | |||||
chr4:6579069
|
T | TCACCATC others(53): Show |
1 | a0003c0044t0002g0132 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.391+576_391+577ins others(60): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579069 | |||||
chr4:6579069
|
TCAC | T | 3 | a0002c0002t0001g0332a0020c0018t0001g0020a0020c0018t0021g0020 | 3 | NA18944.hp2 NA18952.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.391+586_391+588del others(3): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579069 | |||||
chr4:6579069
|
TCACCACC others(86): Show |
T | 2 | a0004c0005t0001g0137a0004c0005t0001g0138 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.391+626_391+718del others(93): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579069 | |||||
chr4:6579072
|
C | CCAG | 5 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(2): Show | 5 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.391+576_391+577ins others(3): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579072 | |||||
chr4:6579075
|
C | T | 1 | a0003c0044t0002g0132 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.391+577C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579075 | ||||||
chr4:6579081
|
C | T | 1 | a0026c0066t0028g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.391+583C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579081 | ||||||
chr4:6579084
|
C | T | 1 | a0001c0003t0002g0320 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.391+586C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579084 | ||||||
chr4:6579085
|
CATCACCA others(32): Show |
C | 1 | a0001c0001t0001g0099 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.391+589_391+627del others(39): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579085 | |||||
chr4:6579087
|
T | C | 4 | a0001c0003t0002g0320a0002c0002t0001g0091a0005c0010t0003g0043others(1): Show | 4 | HG02056.hp2 HG02615.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+589T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579087 | ||||||
chr4:6579087
|
T | TCACCACC others(220): Show |
3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231 | 3 | NA18944.hp1 NA18959.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.391+594_391+595ins others(227): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579087 | |||||
chr4:6579087
|
T | TCACCACC others(499): Show |
1 | a0001c0001t0001g0232 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.391+594_391+595ins others(506): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579087 | |||||
chr4:6579088
|
C | T | 1 | a0002c0002t0001g0091 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.391+590C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579088 | ||||||
chr4:6579090
|
C | T | 2 | a0005c0010t0003g0043a0005c0010t0003g0044 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.391+592C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579090 | ||||||
chr4:6579093
|
T | C | 2 | a0005c0010t0003g0043a0005c0010t0003g0044 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.391+595T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579093 | ||||||
chr4:6579099
|
G | C | 28 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0117others(25): Show | 30 | HG00423.hp2 HG02056.hp2 HG02071.hp1 others(27): Show |
intron_variant | MODIFIER | c.391+601G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579099 | ||||||
chr4:6579099
|
G | GCACCACC others(166): Show |
1 | a0011c0009t0016g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.391+618_391+619ins others(173): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579099 | |||||
chr4:6579099
|
G | GCACCACC others(163): Show |
4 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+618_391+619ins others(170): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579099 | |||||
chr4:6579099
|
G | GCACCACC others(89): Show |
1 | a0012c0022t0001g0315 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.391+618_391+619ins others(96): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579099 | |||||
chr4:6579099
|
GCACCACC others(35): Show |
G | 1 | a0002c0013t0001g0139 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.391+626_391+667del others(42): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579099 | |||||
chr4:6579102
|
CCACCACC others(138): Show |
C | 1 | a0003c0007t0013g0057 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.391+619_391+763del | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579102 | |||||
chr4:6579105
|
C | T | 2 | a0002c0002t0001g0091a0002c0030t0013g0136 | 2 | HG03579.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.391+607C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579105 | ||||||
chr4:6579111
|
T | C | 6 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(3): Show | 6 | HG02723.hp1 HG03486.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.391+613T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579111 | ||||||
chr4:6579111
|
T | TCACCACC others(333): Show |
1 | a0001c0064t0001g0243 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.391+618_391+619ins others(340): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
T | TCACCACC others(139): Show |
1 | a0001c0001t0001g0268 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.391+618_391+619ins others(146): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
T | TCACCACC others(283): Show |
1 | a0001c0001t0001g0244 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.391+618_391+619ins others(290): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
T | TCACCACC others(292): Show |
1 | a0002c0002t0003g0245 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.391+618_391+619ins others(299): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
T | TCACCACC others(220): Show |
1 | a0001c0001t0001g0253 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.391+618_391+619ins others(227): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
T | TCACCACC others(247): Show |
1 | a0001c0001t0001g0251 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.391+618_391+619ins others(254): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
T | TCACCACC others(649): Show |
1 | a0001c0001t0001g0252 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.391+618_391+619ins others(656): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
T | TCACCACC others(808): Show |
1 | a0001c0001t0001g0254 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.391+618_391+619ins others(815): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
T | TCACCACC others(310): Show |
1 | a0031c0063t0001g0256 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.391+618_391+619ins others(317): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
T | TCACCACC others(352): Show |
1 | a0002c0002t0001g0019 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.391+618_391+619ins others(359): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
T | TCACCACC others(364): Show |
1 | a0001c0001t0004g0262 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.391+618_391+619ins others(371): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
T | TCACCACC others(1074): Show |
1 | a0001c0001t0001g0261 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.391+618_391+619ins others(1081): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
T | TCACCACC others(364): Show |
1 | a0001c0001t0001g0266 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.391+618_391+619ins others(371): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
T | TCACCACC others(490): Show |
1 | a0010c0060t0001g0267 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.391+618_391+619ins others(497): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
T | TCACCACC others(712): Show |
1 | a0001c0001t0001g0273 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.391+618_391+619ins others(719): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
T | TCACCACC others(244): Show |
4 | a0001c0001t0001g0277a0001c0001t0001g0285a0001c0001t0004g0278others(1): Show | 4 | HG00642.hp1 HG01361.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.391+618_391+619ins others(251): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
T | TCACCACC others(790): Show |
1 | a0002c0002t0001g0227 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.391+618_391+619ins others(797): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
T | TCACCACC others(643): Show |
1 | a0002c0002t0001g0301 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.391+618_391+619ins others(650): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
T | TCACCACC others(164): Show |
1 | a0001c0001t0001g0305 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.391+618_391+619ins others(171): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
T | TCACCACC others(277): Show |
1 | a0001c0001t0001g0306 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.391+618_391+619ins others(284): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
T | TCACCACC others(96): Show |
1 | a0002c0002t0001g0029 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.391+618_391+619ins others(103): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
T | TCACCACC others(106): Show |
1 | a0002c0002t0001g0316 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.391+618_391+619ins others(113): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579111
|
TCACCATC others(29): Show |
T | 2 | a0001c0055t0002g0122a0002c0002t0009g0037 | 2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.391+625_391+660del others(36): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579111 | |||||
chr4:6579114
|
C | CCACCACC others(391): Show |
1 | a0001c0001t0001g0282 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.391+618_391+619ins others(398): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579114 | |||||
chr4:6579114
|
C | CCACCACC others(367): Show |
1 | a0002c0002t0001g0288 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.391+618_391+619ins others(374): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579114 | |||||
chr4:6579116
|
A | ACCACCAC others(30): Show |
1 | a0001c0001t0001g0314 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.391+618_391+619ins others(37): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579116 | ||||||
chr4:6579116
|
A | ACCACCAC others(73): Show |
2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG01496.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.391+618_391+619ins others(80): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579116 | ||||||
chr4:6579116
|
A | ACCACCAC others(73): Show |
24 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0255others(21): Show | 24 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.391+618_391+619ins others(80): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579116 | ||||||
chr4:6579116
|
A | ACCACCAC others(1532): Show |
1 | a0001c0001t0001g0259 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.391+618_391+619ins others(1539): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579116 | ||||||
chr4:6579117
|
T | C | 52 | a0001c0001t0001g0103a0001c0001t0001g0234a0001c0001t0001g0235others(49): Show | 52 | HG00323.hp2 HG00408.hp2 HG00438.hp2 others(49): Show |
intron_variant | MODIFIER | c.391+619T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579117 | ||||||
chr4:6579120
|
C | CCACCACC others(169): Show |
1 | a0001c0001t0001g0322 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.391+625_391+626ins others(176): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579120 | |||||
chr4:6579120
|
C | CCACCACC others(919): Show |
1 | a0002c0002t0001g0250 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.391+625_391+626ins others(926): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579120 | |||||
chr4:6579123
|
C | CCACCACC others(430): Show |
1 | a0029c0059t0001g0304 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.391+625_391+626ins others(437): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579123 | ||||||
chr4:6579123
|
C | T | 1 | a0002c0002t0001g0029 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.391+625C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579123 | ||||||
chr4:6579124
|
T | C | 167 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(164): Show | 172 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.391+626T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579124 | ||||||
chr4:6579124
|
TACCACCA others(83): Show |
T | 1 | a0015c0019t0002g0142 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.391+655_391+744del others(90): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579124 | |||||
chr4:6579126
|
C | CCACCACC others(163): Show |
1 | a0002c0030t0013g0136 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.391+654_391+655ins others(170): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579126 | |||||
chr4:6579126
|
C | CCACCACC others(337): Show |
1 | a0001c0001t0001g0238 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.391+639_391+640ins others(344): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579126 | |||||
chr4:6579126
|
C | CCACCACC others(614): Show |
1 | a0001c0001t0001g0241 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.391+639_391+640ins others(621): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579126 | |||||
chr4:6579126
|
C | CCACCACC others(619): Show |
1 | a0010c0017t0002g0226 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.391+639_391+640ins others(626): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579126 | |||||
chr4:6579126
|
C | CCACCACC others(388): Show |
1 | a0017c0023t0001g0246 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.391+639_391+640ins others(395): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579126 | |||||
chr4:6579126
|
C | CCACCACC others(478): Show |
1 | a0012c0022t0001g0247 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.391+639_391+640ins others(485): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579126 | |||||
chr4:6579126
|
C | CCACCACC others(340): Show |
1 | a0002c0002t0001g0257 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.391+639_391+640ins others(347): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579126 | |||||
chr4:6579126
|
C | CCACCACC others(340): Show |
1 | a0002c0004t0031g0260 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.391+639_391+640ins others(347): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579126 | |||||
chr4:6579126
|
C | CCACCACC others(631): Show |
1 | a0001c0001t0001g0103 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.391+639_391+640ins others(638): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579126 | |||||
chr4:6579126
|
C | CCACCACC others(337): Show |
1 | a0010c0017t0002g0270 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.391+639_391+640ins others(344): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579126 | |||||
chr4:6579126
|
C | CCACCACC others(340): Show |
1 | a0001c0001t0004g0293 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.391+639_391+640ins others(347): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579126 | |||||
chr4:6579126
|
C | CCACCACC others(337): Show |
1 | a0001c0003t0002g0300 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.391+639_391+640ins others(344): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579126 | |||||
chr4:6579126
|
C | CCACCACC others(331): Show |
1 | a0001c0001t0001g0303 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.391+639_391+640ins others(338): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579126 | |||||
chr4:6579126
|
C | CCACCACC others(30): Show |
1 | a0001c0001t0001g0060 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.391+639_391+640ins others(37): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579126 | |||||
chr4:6579126
|
C | CCACCACC others(250): Show |
1 | a0008c0038t0012g0053 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.391+639_391+640ins others(257): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579126 | |||||
chr4:6579126
|
C | CCACCACC others(216): Show |
1 | a0001c0003t0002g0061 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.391+639_391+640ins others(223): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579126 | |||||
chr4:6579126
|
C | CCACCACC others(414): Show |
1 | a0001c0001t0001g0086 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.391+639_391+640ins others(421): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579126 | |||||
chr4:6579126
|
C | CCACCATC others(76): Show |
4 | a0002c0002t0001g0006a0002c0002t0001g0318a0002c0002t0001g0319others(1): Show | 5 | HG00609.hp1 HG02015.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.391+633_391+634ins others(83): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579126 | |||||
chr4:6579126
|
C | CCACCATC others(391): Show |
1 | a0035c0029t0001g0140 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.391+633_391+634ins others(398): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579126 | |||||
chr4:6579126
|
C | CCACCCTC others(8): Show |
1 | a0003c0044t0002g0132 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.391+632_391+633ins others(15): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579126 | |||||
chr4:6579126
|
C | T | 40 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(37): Show | 40 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.391+628C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579126 | ||||||
chr4:6579129
|
C | CCACCACC others(27): Show |
4 | a0009c0011t0001g0046a0009c0011t0001g0105a0009c0011t0002g0104others(1): Show | 4 | HG03130.hp1 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.391+639_391+640ins others(34): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579129 | |||||
chr4:6579129
|
C | CCACCACC others(51): Show |
1 | a0001c0003t0002g0027 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.391+638_391+639ins others(58): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579129 | |||||
chr4:6579129
|
C | T | 2 | a0001c0001t0001g0099a0002c0002t0001g0316 | 2 | HG00438.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.391+631C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579129 | ||||||
chr4:6579131
|
A | ACCACCAT others(341): Show |
1 | a0001c0001t0001g0296 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.391+639_391+640ins others(348): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579131 | |||||
chr4:6579131
|
A | ACCACCAT others(557): Show |
1 | a0001c0001t0001g0297 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.391+639_391+640ins others(564): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579131 | |||||
chr4:6579131
|
A | ACCACCAT others(1118): Show |
1 | a0001c0001t0001g0298 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.391+639_391+640ins others(1125): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579131 | |||||
chr4:6579132
|
C | CCACCACC others(5): Show |
1 | a0001c0003t0002g0320 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.391+642_391+643ins others(12): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579132 | |||||
chr4:6579132
|
C | CCACCATC others(672): Show |
1 | a0001c0001t0001g0234 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.391+639_391+640ins others(679): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579132 | |||||
chr4:6579132
|
C | CCACCATC others(229): Show |
1 | a0001c0001t0001g0276 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.391+639_391+640ins others(236): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579132 | |||||
chr4:6579132
|
C | CCACCATC others(913): Show |
1 | a0002c0002t0001g0289 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.391+639_391+640ins others(920): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579132 | |||||
chr4:6579132
|
C | CCACCATC others(112): Show |
1 | a0007c0006t0001g0059 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.391+639_391+640ins others(119): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579132 | |||||
chr4:6579132
|
C | CCATCACC others(241): Show |
2 | a0003c0070t0002g0034a0022c0069t0003g0033 | 2 | HG02572.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391+636_391+637ins others(248): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579132 | |||||
chr4:6579132
|
C | T | 20 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0117others(17): Show | 22 | HG00423.hp2 HG02071.hp1 HG02074.hp1 others(19): Show |
intron_variant | MODIFIER | c.391+634C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579132 | ||||||
chr4:6579135
|
C | CCACCACC others(716): Show |
1 | a0001c0003t0002g0233 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.391+642_391+643ins others(723): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579135 | |||||
chr4:6579135
|
C | CCATCACC others(91): Show |
1 | a0001c0001t0001g0302 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.391+639_391+640ins others(98): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579135 | |||||
chr4:6579135
|
C | CCATCACC others(707): Show |
1 | a0001c0001t0001g0258 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.391+639_391+640ins others(714): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579135 | |||||
chr4:6579135
|
C | CCATCACC others(238): Show |
1 | a0001c0003t0003g0264 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.391+639_391+640ins others(245): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579135 | |||||
chr4:6579135
|
C | CCATCACC others(61): Show |
2 | a0001c0001t0001g0311a0001c0001t0001g0312 | 2 | NA18948.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.391+639_391+640ins others(68): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579135 | |||||
chr4:6579135
|
C | CCATCACC others(101): Show |
4 | a0001c0001t0001g0307a0001c0001t0001g0308a0001c0001t0001g0309others(1): Show | 4 | HG00408.hp2 NA18999.hp2 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.391+639_391+640ins others(108): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579135 | |||||
chr4:6579135
|
C | CCATCACC others(98): Show |
1 | a0001c0001t0001g0313 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.391+639_391+640ins others(105): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579135 | |||||
chr4:6579135
|
C | CCATCACC others(375): Show |
1 | a0001c0003t0003g0228 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.391+639_391+640ins others(382): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579135 | |||||
chr4:6579135
|
C | CCATCACC others(307): Show |
1 | a0026c0066t0028g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.391+639_391+640ins others(314): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579135 | |||||
chr4:6579135
|
C | T | 6 | a0001c0001t0001g0099a0001c0001t0001g0252a0001c0001t0001g0254others(3): Show | 6 | HG02074.hp2 HG02300.hp2 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.391+637C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579135 | ||||||
chr4:6579138
|
C | T | 49 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0064others(46): Show | 52 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.391+640C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579138 | ||||||
chr4:6579141
|
T | C | 79 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0064others(76): Show | 82 | HG00408.hp2 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.391+643T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579141 | ||||||
chr4:6579141
|
T | G | 2 | a0001c0001t0001g0099a0002c0002t0001g0091 | 2 | HG02300.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.391+643T>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579141 | ||||||
chr4:6579141
|
T | TCAC | 4 | a0001c0001t0001g0234a0001c0001t0001g0302a0002c0002t0001g0019others(1): Show | 5 | HG01069.hp2 HG01071.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.391+652_391+654dup others(3): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579141 | |||||
chr4:6579144
|
C | T | 13 | a0001c0001t0001g0307a0001c0001t0001g0308a0001c0001t0001g0309others(10): Show | 13 | HG00408.hp2 HG03130.hp1 HG03139.hp2 others(10): Show |
intron_variant | MODIFIER | c.391+646C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579144 | ||||||
chr4:6579147
|
C | G | 1 | a0012c0022t0001g0315 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.391+649C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579147 | ||||||
chr4:6579149
|
A | AC | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0004g0310others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+653dupC | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579149 | |||||
chr4:6579150
|
C | CCCTT | 38 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0064others(35): Show | 41 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.391+653_391+654ins others(4): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579150 | |||||
chr4:6579150
|
C | CCCTTCAC others(52): Show |
6 | a0001c0054t0002g0220a0006c0050t0026g0224a0011c0009t0002g0048others(3): Show | 6 | HG02451.hp1 HG02723.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.391+653_391+654ins others(59): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579150 | |||||
chr4:6579151
|
C | T | 4 | a0002c0002t0001g0215a0002c0002t0001g0216a0002c0002t0001g0217others(1): Show | 4 | HG00140.hp1 HG01261.hp1 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+653C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579151 | ||||||
chr4:6579152
|
A | T | 4 | a0001c0001t0001g0239a0001c0001t0001g0240a0001c0001t0004g0310others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+654A>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579152 | ||||||
chr4:6579152
|
ATCACCAT others(58): Show |
A | 1 | a0042c0043t0030g0089 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.391+655_391+719del others(65): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579152 | ||||||
chr4:6579153
|
T | C | 92 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0064others(89): Show | 95 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.391+655T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579153 | ||||||
chr4:6579155
|
A | C | 2 | a0001c0001t0001g0317a0001c0003t0002g0054 | 2 | HG03669.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.391+657A>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579155 | ||||||
chr4:6579156
|
C | T | 1 | a0001c0001t0001g0306 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.391+658C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579156 | ||||||
chr4:6579158
|
A | T | 2 | a0001c0001t0001g0317a0001c0003t0002g0054 | 2 | HG03669.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.391+660A>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579158 | ||||||
chr4:6579159
|
T | C | 38 | a0001c0001t0001g0234a0001c0001t0001g0235a0001c0001t0001g0238others(35): Show | 39 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.391+661T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579159 | ||||||
chr4:6579159
|
T | TCACCACC others(1230): Show |
1 | a0013c0052t0003g0225 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.391+674_391+675ins others(1237): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579159 | |||||
chr4:6579162
|
C | CCACCACC others(209): Show |
16 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0117others(13): Show | 18 | HG00423.hp2 HG02071.hp1 HG02074.hp1 others(15): Show |
intron_variant | MODIFIER | c.391+681_391+682ins others(216): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579162 | |||||
chr4:6579162
|
C | CCACCACC others(206): Show |
1 | a0002c0002t0004g0110 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.391+681_391+682ins others(213): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579162 | |||||
chr4:6579162
|
C | CCACCCTT others(63): Show |
1 | a0001c0001t0001g0235 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.391+668_391+669ins others(70): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579162 | |||||
chr4:6579162
|
C | T | 24 | a0001c0001t0023g0211a0001c0003t0002g0202a0002c0002t0001g0018others(21): Show | 26 | HG00738.hp1 HG01255.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.391+664C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579162 | ||||||
chr4:6579165
|
C | G | 2 | a0003c0070t0002g0034a0022c0069t0003g0033 | 2 | HG02572.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391+667C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579165 | ||||||
chr4:6579168
|
C | CCACCACC others(17): Show |
1 | a0037c0047t0027g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.391+694_391+717dup others(24): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579168 | |||||
chr4:6579168
|
C | CCACCAT | 4 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+675_391+676ins others(6): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579168 | |||||
chr4:6579168
|
C | CCACCATC others(244): Show |
1 | a0011c0009t0016g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.391+675_391+676ins others(251): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579168 | |||||
chr4:6579168
|
C | T | 3 | a0001c0001t0001g0322a0001c0003t0002g0054a0002c0002t0001g0019 | 4 | HG01069.hp2 HG01071.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+670C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579168 | ||||||
chr4:6579171
|
C | CCACCATC others(268): Show |
1 | a0001c0001t0004g0310 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.391+678_391+679ins others(275): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579171 | |||||
chr4:6579171
|
C | CCAT | 55 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(52): Show | 56 | HG00408.hp1 HG00423.hp1 HG00597.hp2 others(53): Show |
intron_variant | MODIFIER | c.391+675_391+676ins others(3): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579171 | |||||
chr4:6579171
|
C | CCCTT | 11 | a0001c0001t0001g0307a0001c0001t0001g0308a0001c0001t0001g0309others(8): Show | 11 | HG00408.hp2 HG03130.hp1 HG03139.hp2 others(8): Show |
intron_variant | MODIFIER | c.391+674_391+675ins others(4): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579171 | |||||
chr4:6579171
|
C | T | 4 | a0001c0001t0001g0244a0001c0001t0001g0268a0001c0003t0002g0061others(1): Show | 4 | HG02129.hp1 NA18965.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+673C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579171 | ||||||
chr4:6579174
|
C | CCACCACC others(227): Show |
1 | a0002c0002t0001g0111 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.391+681_391+682ins others(234): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579174 | |||||
chr4:6579174
|
C | T | 37 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0064others(34): Show | 40 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.391+676C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579174 | ||||||
chr4:6579177
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.391+679C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579177 | ||||||
chr4:6579179
|
A | ACCACCAC others(276): Show |
1 | a0002c0002t0001g0109 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.391+681_391+682ins others(283): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579179 | ||||||
chr4:6579179
|
A | T | 2 | a0001c0001t0001g0252a0001c0001t0001g0254 | 2 | NA18990.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.391+681A>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579179 | ||||||
chr4:6579180
|
T | C | 72 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(69): Show | 76 | HG00438.hp1 HG00558.hp1 HG00558.hp2 others(73): Show |
intron_variant | MODIFIER | c.391+682T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579180 | ||||||
chr4:6579180
|
T | TCAC | 16 | a0001c0001t0001g0234a0001c0001t0001g0239a0001c0001t0001g0240others(13): Show | 16 | HG00323.hp2 HG00408.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.391+685_391+687dup others(3): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579180 | |||||
chr4:6579184
|
C | CACCACCA others(45): Show |
1 | a0002c0002t0001g0242 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.391+687_391+688ins others(52): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579184 | |||||
chr4:6579186
|
T | C | 65 | a0001c0001t0001g0060a0001c0001t0001g0103a0001c0001t0001g0229others(62): Show | 66 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.391+688T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579186 | ||||||
chr4:6579189
|
C | CCAT | 4 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+693_391+694ins others(3): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579189 | |||||
chr4:6579189
|
C | T | 4 | a0001c0001t0001g0060a0001c0001t0001g0276a0002c0002t0001g0109others(1): Show | 4 | HG01168.hp1 HG02055.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.391+691C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579189 | ||||||
chr4:6579192
|
G | C | 109 | a0001c0001t0001g0060a0001c0001t0001g0086a0001c0001t0001g0229others(106): Show | 110 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.391+694G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579192 | ||||||
chr4:6579192
|
G | T | 43 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0064others(40): Show | 46 | HG00438.hp1 HG00609.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.391+694G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579192 | ||||||
chr4:6579192
|
GCACCACC others(14): Show |
G | 1 | a0002c0002t0001g0143 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.391+706_391+726del others(21): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579192 | |||||
chr4:6579194
|
A | T | 1 | a0002c0002t0001g0091 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.391+696A>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579194 | ||||||
chr4:6579195
|
C | T | 21 | a0001c0001t0001g0258a0001c0001t0001g0266a0001c0001t0001g0307others(18): Show | 21 | HG00408.hp2 HG02257.hp1 HG02300.hp1 others(18): Show |
intron_variant | MODIFIER | c.391+697C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579195 | ||||||
chr4:6579197
|
A | C | 1 | a0033c0062t0001g0102 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.391+699A>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579197 | ||||||
chr4:6579201
|
C | T | 7 | a0001c0001t0001g0086a0001c0001t0001g0244a0001c0001t0001g0268others(4): Show | 7 | HG00558.hp2 HG00735.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.391+703C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579201 | ||||||
chr4:6579203
|
A | T | 2 | a0001c0001t0001g0317a0012c0022t0001g0315 | 2 | HG03017.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.391+705A>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579203 | ||||||
chr4:6579204
|
T | C | 42 | a0001c0001t0001g0086a0001c0001t0001g0234a0001c0001t0001g0238others(39): Show | 42 | HG00323.hp2 HG00408.hp1 HG00438.hp2 others(39): Show |
intron_variant | MODIFIER | c.391+706T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579204 | ||||||
chr4:6579204
|
T | TCACCACC others(29): Show |
1 | a0001c0001t0001g0275 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.391+711_391+712ins others(36): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579204 | |||||
chr4:6579207
|
C | T | 1 | a0011c0009t0016g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.391+709C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579207 | ||||||
chr4:6579207
|
CCAT | C | 10 | a0001c0001t0001g0022a0001c0001t0001g0088a0001c0001t0001g0307others(7): Show | 10 | HG00408.hp2 HG01358.hp2 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.391+712_391+714del others(3): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579207 | |||||
chr4:6579210
|
T | C | 115 | a0001c0001t0001g0009a0001c0001t0001g0060a0001c0001t0001g0064others(112): Show | 122 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(119): Show |
intron_variant | MODIFIER | c.391+712T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579210 | ||||||
chr4:6579210
|
T | TCAC | 4 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+730_391+732dup others(3): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579210 | |||||
chr4:6579210
|
TCAC | T | 4 | a0001c0001t0001g0302a0003c0007t0009g0041a0003c0007t0010g0007others(1): Show | 5 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.391+730_391+732del others(3): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579210 | |||||
chr4:6579213
|
C | CCAG | 4 | a0009c0011t0001g0046a0009c0011t0001g0105a0009c0011t0002g0104others(1): Show | 4 | HG03130.hp1 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.391+717_391+718ins others(3): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579213 | |||||
chr4:6579213
|
C | T | 1 | a0001c0001t0001g0103 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.391+715C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579213 | ||||||
chr4:6579216
|
C | CCAT | 23 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(20): Show | 23 | HG00323.hp2 HG00642.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.391+720_391+721ins others(3): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579216 | |||||
chr4:6579216
|
C | T | 3 | a0001c0001t0001g0234a0001c0001t0001g0330a0010c0060t0001g0267 | 3 | HG01175.hp2 HG01433.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.391+718C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579216 | ||||||
chr4:6579218
|
A | C | 1 | a0042c0043t0030g0089 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.391+720A>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579218 | ||||||
chr4:6579219
|
C | T | 11 | a0001c0001t0001g0258a0001c0001t0001g0277a0001c0001t0001g0285others(8): Show | 11 | HG00438.hp2 HG00642.hp1 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.391+721C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579219 | ||||||
chr4:6579221
|
A | T | 1 | a0042c0043t0030g0089 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.391+723A>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579221 | ||||||
chr4:6579222
|
C | CCACCACC others(8): Show |
1 | a0001c0001t0001g0259 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.391+732_391+733ins others(15): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579222 | |||||
chr4:6579222
|
C | CCACCACC others(93): Show |
3 | a0002c0002t0001g0215a0002c0002t0001g0216a0002c0004t0002g0214 | 3 | HG00140.hp1 HG01261.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.391+732_391+733ins others(100): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579222 | |||||
chr4:6579222
|
C | CCACCACC others(168): Show |
1 | a0002c0002t0001g0217 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.391+732_391+733ins others(175): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579222 | |||||
chr4:6579222
|
C | T | 33 | a0001c0001t0001g0009a0001c0001t0001g0064a0001c0001t0001g0065others(30): Show | 36 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.391+724C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579222 | ||||||
chr4:6579225
|
C | T | 15 | a0001c0001t0001g0022a0001c0001t0001g0088a0001c0001t0001g0244others(12): Show | 15 | HG00408.hp1 HG00558.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.391+727C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579225 | ||||||
chr4:6579228
|
C | T | 1 | a0001c0001t0001g0269 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.391+730C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579228 | ||||||
chr4:6579231
|
T | C | 86 | a0001c0001t0001g0009a0001c0001t0001g0064a0001c0001t0001g0065others(83): Show | 90 | HG00408.hp1 HG00423.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.391+733T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579231 | ||||||
chr4:6579231
|
T | G | 1 | a0021c0020t0002g0049 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.391+733T>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579231 | ||||||
chr4:6579237
|
C | G | 2 | a0021c0020t0002g0045a0040c0039t0007g0050 | 2 | HG02280.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.391+739C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579237 | ||||||
chr4:6579237
|
C | T | 29 | a0001c0001t0001g0060a0001c0001t0001g0234a0001c0001t0001g0236others(26): Show | 29 | HG00423.hp1 HG00597.hp2 HG00733.hp2 others(26): Show |
intron_variant | MODIFIER | c.391+739C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579237 | ||||||
chr4:6579240
|
C | T | 4 | a0001c0001t0001g0086a0010c0060t0001g0267a0024c0067t0025g0031others(1): Show | 4 | HG00735.hp1 HG01993.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.391+742C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579240 | ||||||
chr4:6579242
|
A | ATCACCAC others(73): Show |
1 | a0001c0001t0001g0282 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.391+744_391+745ins others(80): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579242 | ||||||
chr4:6579242
|
A | ATCACCAT others(4): Show |
1 | a0021c0020t0002g0049 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.391+744_391+745ins others(11): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579242 | ||||||
chr4:6579242
|
AC | A | 17 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0103others(14): Show | 18 | HG00558.hp1 HG01069.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.391+747delC | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579242 | |||||
chr4:6579243
|
C | A | 2 | a0001c0001t0001g0282a0021c0020t0002g0049 | 2 | HG00673.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.391+745C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579243 | ||||||
chr4:6579243
|
C | CCA | 27 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0001g0244others(24): Show | 27 | HG00323.hp2 HG00597.hp2 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.391+746_391+747ins others(2): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
C | CCACCA | 6 | a0001c0001t0001g0269a0001c0001t0001g0296a0001c0001t0001g0297others(3): Show | 6 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(3): Show |
intron_variant | MODIFIER | c.391+746_391+747ins others(5): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
C | CCACCACC others(103): Show |
1 | a0001c0001t0001g0251 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.391+746_391+747ins others(110): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
C | CCACCACC others(100): Show |
1 | a0001c0001t0001g0253 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.391+746_391+747ins others(107): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
C | CCACCACC others(467): Show |
1 | a0002c0002t0003g0245 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.391+746_391+747ins others(474): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
C | CCACCACC others(94): Show |
4 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(1): Show | 4 | NA18944.hp1 NA18955.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+746_391+747ins others(101): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
C | CCACCACC others(292): Show |
1 | a0001c0001t0001g0086 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.391+746_391+747ins others(299): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
C | CCACCACC others(79): Show |
1 | a0001c0001t0001g0272 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.391+746_391+747ins others(86): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
C | CCACCATC others(10): Show |
2 | a0021c0020t0002g0045a0040c0039t0007g0050 | 2 | HG02280.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.391+746_391+747ins others(17): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
C | CCATCACC others(31): Show |
1 | a0001c0001t0001g0255 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.391+746_391+747ins others(38): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
C | CCATCACC others(298): Show |
1 | a0006c0016t0003g0271 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.391+746_391+747ins others(305): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
C | CCATCACC others(121): Show |
1 | a0001c0001t0001g0283 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.391+746_391+747ins others(128): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
C | CCATCACC others(259): Show |
3 | a0001c0001t0001g0280a0001c0001t0004g0281a0006c0057t0001g0279 | 3 | HG02027.hp2 NA18949.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.391+746_391+747ins others(266): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
C | CCATCACC others(247): Show |
1 | a0002c0002t0001g0028 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.391+746_391+747ins others(254): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
C | CCATCACC others(244): Show |
1 | a0001c0001t0001g0286 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.391+746_391+747ins others(251): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
C | CCATCACC others(505): Show |
1 | a0002c0002t0001g0287 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.391+746_391+747ins others(512): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
C | CCATCACC others(631): Show |
1 | a0001c0001t0001g0290 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.391+746_391+747ins others(638): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
C | CCATCACC others(658): Show |
1 | a0001c0001t0001g0314 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.391+746_391+747ins others(665): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
C | CCATCACC others(703): Show |
1 | a0001c0003t0002g0291 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.391+746_391+747ins others(710): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
C | CCATCACC others(703): Show |
1 | a0001c0001t0001g0292 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.391+746_391+747ins others(710): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
C | CCATCACC others(271): Show |
4 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0295others(1): Show | 4 | HG01070.hp1 HG01070.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.391+746_391+747ins others(278): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
C | CCATCACC others(256): Show |
1 | a0001c0001t0001g0263 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.391+746_391+747ins others(263): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
CCCTT | C | 8 | a0001c0001t0001g0234a0002c0002t0001g0091a0009c0011t0001g0046others(5): Show | 8 | HG01175.hp2 HG02258.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.391+747_391+750del others(4): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
CCCTTCAC others(39): Show |
C | 3 | a0001c0001t0001g0022a0001c0001t0001g0088a0001c0001t0019g0052 | 3 | HG01358.hp2 HG01496.hp2 NA19001.hp2 |
intron_variant | MODIFIER | c.391+747_391+792del others(46): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579243
|
CCCTTCAC others(51): Show |
C | 27 | a0001c0001t0001g0009a0001c0001t0001g0064a0001c0001t0001g0065others(24): Show | 30 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.391+747_391+804del others(58): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579243 | |||||
chr4:6579246
|
T | A | 85 | a0001c0001t0001g0060a0001c0001t0001g0086a0001c0001t0001g0092others(82): Show | 86 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.391+748T>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579246 | ||||||
chr4:6579247
|
T | C | 27 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0238others(24): Show | 27 | HG00323.hp2 HG00558.hp1 HG00642.hp2 others(24): Show |
intron_variant | MODIFIER | c.391+749T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579247 | ||||||
chr4:6579247
|
T | TCACCACC others(123): Show |
2 | a0005c0010t0003g0043a0005c0010t0003g0044 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.391+784_391+785ins others(130): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579247 | |||||
chr4:6579250
|
C | T | 2 | a0001c0001t0001g0234a0002c0002t0001g0250 | 2 | HG01175.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.391+752C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579250 | ||||||
chr4:6579253
|
C | T | 3 | a0001c0001t0001g0285a0001c0001t0018g0284a0002c0002t0001g0091 | 3 | HG00642.hp1 HG01361.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.391+755C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579253 | ||||||
chr4:6579256
|
T | C | 23 | a0001c0001t0001g0060a0001c0001t0001g0234a0001c0001t0001g0235others(20): Show | 24 | HG00597.hp2 HG00609.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.391+758T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579256 | ||||||
chr4:6579256
|
T | TCACCACC others(185): Show |
1 | a0035c0029t0001g0140 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.391+784_391+785ins others(192): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579256 | |||||
chr4:6579259
|
C | CCACCACC others(384): Show |
1 | a0001c0001t0001g0261 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.391+772_391+773ins others(391): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579259 | |||||
chr4:6579259
|
C | CCACCACC others(447): Show |
1 | a0001c0001t0001g0235 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.391+772_391+773ins others(454): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579259 | |||||
chr4:6579259
|
C | CCACCACC others(672): Show |
3 | a0002c0002t0001g0006a0002c0002t0001g0318a0002c0002t0004g0006 | 4 | HG00609.hp1 HG02015.hp1 NA18949.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+772_391+773ins others(679): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579259 | |||||
chr4:6579259
|
C | CCACCACC others(1071): Show |
1 | a0002c0002t0001g0319 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.391+772_391+773ins others(1078): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579259 | |||||
chr4:6579259
|
C | CCACCACC others(38): Show |
1 | a0001c0001t0012g0030 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.391+784_391+785ins others(45): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579259 | |||||
chr4:6579259
|
C | CCACCACC others(50): Show |
22 | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0160others(19): Show | 28 | HG00639.hp1 HG01109.hp2 HG01243.hp2 others(25): Show |
intron_variant | MODIFIER | c.391+784_391+785ins others(57): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579259 | |||||
chr4:6579259
|
C | CCACCAT | 12 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0001g0303others(9): Show | 12 | HG00323.hp2 HG00642.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.391+766_391+767ins others(6): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579259 | |||||
chr4:6579259
|
C | CCATCACC others(14): Show |
1 | a0001c0001t0001g0090 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.391+763_391+764ins others(21): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579259 | |||||
chr4:6579259
|
C | T | 3 | a0002c0004t0003g0323a0003c0041t0002g0076a0006c0016t0003g0271 | 3 | HG01884.hp2 HG02809.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.391+761C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579259 | ||||||
chr4:6579259
|
CCACCACC others(5): Show |
C | 1 | a0007c0006t0001g0059 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.391+779_391+790del others(12): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579259 | |||||
chr4:6579262
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.391+764C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579262 | ||||||
chr4:6579264
|
A | ACCACCAT others(174): Show |
1 | a0011c0009t0002g0048 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.391+784_391+785ins others(181): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579264 | |||||
chr4:6579264
|
A | ACCACCAT others(329): Show |
1 | a0005c0021t0001g0008 | 2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.391+784_391+785ins others(336): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579264 | |||||
chr4:6579265
|
C | T | 3 | a0001c0001t0001g0107a0001c0001t0001g0117a0002c0002t0001g0194 | 3 | HG00597.hp1 NA19083.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.391+767C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579265 | ||||||
chr4:6579268
|
C | T | 2 | a0024c0067t0025g0031a0025c0068t0001g0032 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.391+770C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579268 | ||||||
chr4:6579271
|
T | C | 70 | a0001c0001t0001g0107a0001c0001t0001g0117a0001c0001t0001g0229others(67): Show | 73 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.391+773T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579271 | ||||||
chr4:6579271
|
T | TCACCACC others(149): Show |
1 | a0001c0001t0001g0252 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.391+784_391+785ins others(156): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579271 | |||||
chr4:6579271
|
T | TCACCACC others(173): Show |
2 | a0001c0001t0001g0285a0001c0001t0018g0284 | 2 | HG00642.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.391+784_391+785ins others(180): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579271 | |||||
chr4:6579271
|
T | TCACCACC others(242): Show |
1 | a0001c0001t0001g0103 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.391+781_391+782ins others(249): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579271 | |||||
chr4:6579274
|
C | CCACCATC others(584): Show |
1 | a0001c0001t0001g0299 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.391+781_391+782ins others(591): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579274 | |||||
chr4:6579274
|
CCACCACC others(8): Show |
C | 1 | a0015c0019t0002g0142 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.391+785_391+799del others(15): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579274 | |||||
chr4:6579277
|
C | CCAT | 30 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0229others(27): Show | 31 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.391+781_391+782ins others(3): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579277 | |||||
chr4:6579277
|
C | T | 6 | a0001c0001t0001g0107a0001c0001t0001g0117a0001c0001t0001g0266others(3): Show | 6 | HG02300.hp1 NA18747.hp2 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.391+779C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579277 | ||||||
chr4:6579280
|
C | T | 3 | a0001c0001t0001g0234a0001c0001t0001g0273a0001c0001t0001g0290 | 3 | HG00423.hp1 HG01175.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.391+782C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579280 | ||||||
chr4:6579283
|
T | C | 29 | a0001c0001t0001g0090a0001c0001t0001g0092a0001c0001t0001g0093others(26): Show | 29 | HG00423.hp1 HG00558.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.391+785T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579283 | ||||||
chr4:6579286
|
C | T | 1 | a0001c0001t0001g0290 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.391+788C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579286 | ||||||
chr4:6579289
|
T | C | 55 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0107others(52): Show | 56 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.391+791T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579289 | ||||||
chr4:6579289
|
T | TCAC | 23 | a0001c0001t0001g0103a0001c0001t0001g0235a0001c0001t0001g0238others(20): Show | 24 | HG00323.hp2 HG00609.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.391+800_391+802dup others(3): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579289 | |||||
chr4:6579289
|
T | TCACCACC others(44): Show |
1 | a0001c0001t0001g0086 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.391+802_391+803ins others(51): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579289 | |||||
chr4:6579289
|
T | TCACCACC others(236): Show |
1 | a0001c0001t0001g0244 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.391+802_391+803ins others(243): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579289 | |||||
chr4:6579289
|
T | TCACCACC others(395): Show |
1 | a0002c0002t0001g0242 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.391+802_391+803ins others(402): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579289 | |||||
chr4:6579289
|
T | TCACCACC others(368): Show |
1 | a0001c0001t0001g0317 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.391+802_391+803ins others(375): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579289 | |||||
chr4:6579289
|
T | TCACCACC others(233): Show |
1 | a0001c0001t0001g0268 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.391+802_391+803ins others(240): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579289 | |||||
chr4:6579289
|
T | TCACCACC others(218): Show |
1 | a0001c0001t0001g0275 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.391+802_391+803ins others(225): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579289 | |||||
chr4:6579289
|
T | TCACCACC others(221): Show |
1 | a0001c0003t0003g0264 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.391+802_391+803ins others(228): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579289 | |||||
chr4:6579289
|
T | TCACCACC others(416): Show |
2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.391+802_391+803ins others(423): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579289 | |||||
chr4:6579289
|
T | TCACCACC others(389): Show |
1 | a0001c0001t0001g0329 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.391+802_391+803ins others(396): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579289 | |||||
chr4:6579289
|
T | TCACCACC others(23): Show |
1 | a0002c0030t0013g0136 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.391+820_391+821ins others(30): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579289 | |||||
chr4:6579289
|
TCACCACC others(11): Show |
T | 3 | a0002c0004t0002g0198a0003c0036t0002g0036a0014c0012t0002g0197 | 3 | HG02559.hp1 HG03041.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.391+821_391+838del others(18): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579289 | |||||
chr4:6579289
|
TCACCACC others(29): Show |
T | 1 | a0002c0004t0003g0196 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.391+803_391+838del others(36): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579289 | |||||
chr4:6579292
|
C | T | 3 | a0001c0001t0001g0266a0001c0001t0004g0262a0002c0002t0001g0301 | 3 | HG02300.hp1 NA18747.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.391+794C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579292 | ||||||
chr4:6579295
|
C | CCACCACC others(392): Show |
1 | a0001c0001t0001g0321 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.391+802_391+803ins others(399): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579295 | |||||
chr4:6579295
|
C | CCACCACC others(548): Show |
1 | a0001c0001t0001g0302 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.391+802_391+803ins others(555): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579295 | |||||
chr4:6579295
|
C | T | 5 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0269others(2): Show | 5 | HG02080.hp1 HG02155.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.391+797C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579295 | ||||||
chr4:6579298
|
C | T | 30 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(27): Show | 31 | HG00438.hp2 HG00558.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.391+800C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579298 | ||||||
chr4:6579301
|
T | C | 68 | a0001c0001t0001g0022a0001c0001t0001g0086a0001c0001t0001g0088others(65): Show | 70 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.391+803T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579301 | ||||||
chr4:6579304
|
C | T | 17 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0255others(14): Show | 17 | HG00408.hp2 HG00438.hp1 HG00733.hp2 others(14): Show |
intron_variant | MODIFIER | c.391+806C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579304 | ||||||
chr4:6579307
|
C | CCACCACC others(479): Show |
1 | a0002c0002t0001g0288 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.391+820_391+821ins others(486): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579307 | |||||
chr4:6579307
|
C | CCACCACC others(23): Show |
1 | a0002c0002t0009g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.391+832_391+833ins others(30): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579307 | |||||
chr4:6579307
|
C | CCACCATC others(221): Show |
1 | a0001c0001t0001g0272 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.391+814_391+815ins others(228): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579307 | |||||
chr4:6579307
|
C | CCAT | 49 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0234others(46): Show | 52 | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.391+811_391+812ins others(3): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579307 | |||||
chr4:6579307
|
C | CCATCACC others(143): Show |
1 | a0001c0003t0002g0320 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.391+811_391+812ins others(150): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579307 | |||||
chr4:6579307
|
C | T | 34 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(31): Show | 35 | HG00423.hp1 HG00438.hp2 HG00558.hp2 others(32): Show |
intron_variant | MODIFIER | c.391+809C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579307 | ||||||
chr4:6579310
|
C | CCACCACC others(2): Show |
4 | a0001c0001t0001g0090a0001c0001t0001g0099a0001c0003t0002g0058others(1): Show | 4 | HG02300.hp2 HG02486.hp1 NA18954.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+821_391+829dup others(9): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579310 | |||||
chr4:6579310
|
C | CCACCACC others(32): Show |
1 | a0001c0003t0002g0061 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.391+844_391+845ins others(39): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579310 | |||||
chr4:6579310
|
C | CCACCACC others(95): Show |
1 | a0033c0062t0001g0102 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.391+835_391+836ins others(102): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579310 | |||||
chr4:6579310
|
C | T | 32 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0064others(29): Show | 35 | HG00609.hp2 HG00621.hp1 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.391+812C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579310 | ||||||
chr4:6579313
|
C | T | 16 | a0001c0001t0001g0107a0001c0001t0001g0117a0001c0001t0001g0307others(13): Show | 16 | HG00408.hp2 HG00438.hp1 HG00735.hp2 others(13): Show |
intron_variant | MODIFIER | c.391+815C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579313 | ||||||
chr4:6579316
|
C | T | 3 | a0001c0001t0001g0101a0001c0001t0001g0302a0001c0001t0001g0321 | 3 | HG04184.hp1 NA18999.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.391+818C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579316 | ||||||
chr4:6579319
|
T | C | 79 | a0001c0001t0001g0060a0001c0001t0001g0101a0001c0001t0001g0103others(76): Show | 82 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.391+821T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579319 | ||||||
chr4:6579319
|
T | TCAC | 4 | a0001c0001t0001g0107a0001c0001t0001g0117a0003c0070t0002g0034others(1): Show | 4 | HG02572.hp2 NA19083.hp2 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.391+842_391+844dup others(3): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579319 | |||||
chr4:6579319
|
T | TCACCATC others(2): Show |
15 | a0001c0001t0001g0115a0002c0002t0001g0013a0002c0002t0001g0014others(12): Show | 17 | HG00423.hp2 HG02071.hp1 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.391+826_391+827ins others(9): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579319 | |||||
chr4:6579319
|
TCAC | T | 14 | a0001c0054t0002g0220a0005c0010t0003g0043a0005c0010t0003g0044others(11): Show | 14 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.391+842_391+844del others(3): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579319 | |||||
chr4:6579319
|
TCACCAC | T | 7 | a0001c0001t0001g0266a0001c0001t0004g0262a0002c0002t0001g0190others(4): Show | 7 | HG00099.hp2 HG01069.hp1 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.391+839_391+844del others(6): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579319 | |||||
chr4:6579322
|
C | CCACCACC others(50): Show |
1 | a0002c0002t0001g0163 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.391+868_391+869ins others(57): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579322 | |||||
chr4:6579322
|
C | T | 2 | a0005c0021t0001g0008a0011c0009t0002g0048 | 3 | HG01891.hp2 HG02723.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.391+824C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579322 | ||||||
chr4:6579325
|
C | CCACCACC others(761): Show |
1 | a0010c0060t0001g0267 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.391+844_391+845ins others(768): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCACCACC others(495): Show |
1 | a0001c0001t0001g0296 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.391+844_391+845ins others(502): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCACCACC others(95): Show |
1 | a0001c0001t0001g0255 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.391+844_391+845ins others(102): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCACCACC others(296): Show |
1 | a0001c0001t0001g0248 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.391+838_391+839ins others(303): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCACCACC others(401): Show |
1 | a0012c0022t0001g0315 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.391+838_391+839ins others(408): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCACCACC others(362): Show |
1 | a0002c0002t0001g0316 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.391+838_391+839ins others(369): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCACCACC others(401): Show |
1 | a0001c0001t0001g0249 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.391+838_391+839ins others(408): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCACCACC others(410): Show |
4 | a0001c0001t0001g0307a0001c0001t0001g0308a0001c0001t0001g0311others(1): Show | 4 | NA18948.hp2 NA18975.hp1 NA19080.hp1 others(1): Show |
intron_variant | MODIFIER | c.391+838_391+839ins others(417): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCACCACC others(407): Show |
2 | a0001c0001t0001g0309a0001c0001t0001g0313 | 2 | HG00408.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.391+838_391+839ins others(414): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCACCACC others(461): Show |
1 | a0002c0002t0001g0029 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.391+838_391+839ins others(468): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCACCACC others(503): Show |
1 | a0001c0001t0004g0310 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.391+838_391+839ins others(510): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCACCACC others(194): Show |
2 | a0001c0001t0001g0277a0001c0001t0004g0278 | 2 | NA18941.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.391+835_391+836ins others(201): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCACCACC others(29): Show |
1 | a0002c0002t0001g0227 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.391+835_391+836ins others(36): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCACCATC others(167): Show |
1 | a0001c0001t0001g0254 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.391+832_391+833ins others(174): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCACCATC others(506): Show |
1 | a0002c0002t0001g0250 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.391+832_391+833ins others(513): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCACCATC others(417): Show |
1 | a0001c0001t0001g0259 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.391+832_391+833ins others(424): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCACCATC others(99): Show |
1 | a0002c0004t0002g0219 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.391+832_391+833ins others(106): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCACCATC others(192): Show |
1 | a0002c0002t0001g0193 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.391+832_391+833ins others(199): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCACCATC others(386): Show |
1 | a0001c0064t0001g0243 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.391+832_391+833ins others(393): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCACCATC others(272): Show |
1 | a0001c0001t0001g0269 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.391+832_391+833ins others(279): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCACCATC others(287): Show |
1 | a0001c0003t0002g0265 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.391+832_391+833ins others(294): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCACCATC others(284): Show |
1 | a0001c0001t0001g0305 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.391+832_391+833ins others(291): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCATCACC others(485): Show |
1 | a0002c0002t0001g0274 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.391+829_391+830ins others(492): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCATCACC others(68): Show |
1 | a0001c0001t0001g0273 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.391+829_391+830ins others(75): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCATCACC others(215): Show |
1 | a0001c0003t0003g0228 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.391+829_391+830ins others(222): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | CCATCACC others(614): Show |
1 | a0001c0001t0001g0276 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.391+829_391+830ins others(621): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579325 | |||||
chr4:6579325
|
C | T | 73 | a0001c0001t0001g0103a0001c0001t0001g0229a0001c0001t0001g0230others(70): Show | 75 | HG00323.hp2 HG00408.hp1 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.391+827C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579325 | ||||||
chr4:6579331
|
C | CCACCACC others(87): Show |
1 | a0011c0009t0016g0026 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.391+856_391+857ins others(94): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579331 | |||||
chr4:6579331
|
C | T | 1 | a0002c0002t0009g0025 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.391+833C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579331 | ||||||
chr4:6579340
|
CCAT | C | 4 | a0001c0055t0002g0122a0002c0002t0009g0037a0013c0053t0014g0040others(1): Show | 4 | HG02723.hp1 HG02965.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.391+845_391+847del others(3): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579340 | |||||
chr4:6579343
|
T | C | 3 | a0002c0030t0013g0136a0024c0067t0025g0031a0025c0068t0001g0032 | 3 | HG02258.hp1 HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.391+845T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579343 | ||||||
chr4:6579349
|
T | C | 2 | a0001c0001t0001g0302a0001c0003t0002g0162 | 2 | HG03710.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.391+851T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579349 | ||||||
chr4:6579355
|
CCACCAT | C | 7 | a0001c0055t0002g0122a0002c0002t0009g0037a0003c0007t0009g0041others(4): Show | 8 | HG02258.hp2 HG02559.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.391+869_391+874del others(6): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579355 | |||||
chr4:6579361
|
T | TCACCACC others(60): Show |
2 | a0024c0067t0025g0031a0025c0068t0001g0032 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.391+868_391+869ins others(67): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579361 | |||||
chr4:6579361
|
T | TCACCATC others(71): Show |
1 | a0001c0003t0002g0162 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.391+884_391+885ins others(78): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579361 | |||||
chr4:6579361
|
T | TCACCATC others(50): Show |
1 | a0008c0038t0012g0053 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.391+880_391+881ins others(57): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579361 | |||||
chr4:6579383
|
T | C | 168 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(165): Show | 175 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.391+885T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579383 | ||||||
chr4:6579395
|
T | TCAC | 129 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0115others(126): Show | 133 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.391+909_391+911dup others(3): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579395 | |||||
chr4:6579437
|
C | A | 1 | a0002c0002t0001g0194 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.391+939C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579437 | ||||||
chr4:6579440
|
T | A | 1 | a0002c0002t0001g0194 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.391+942T>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579440 | ||||||
chr4:6579441
|
T | C | 1 | a0002c0002t0001g0194 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.391+943T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579441 | ||||||
chr4:6579442
|
CACCATCA others(39): Show |
C | 2 | a0002c0004t0003g0055a0002c0004t0003g0056 | 2 | HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.391+960_391+1005de others(47): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579442 | |||||
chr4:6579447
|
T | C | 1 | a0002c0002t0001g0194 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.391+949T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579447 | ||||||
chr4:6579459
|
T | A | 1 | a0002c0002t0001g0194 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.391+961T>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579459 | ||||||
chr4:6579485
|
CACTACCA others(17): Show |
C | 1 | a0001c0001t0001g0249 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.391+1006_391+1029d others(26): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579485 | |||||
chr4:6579490
|
C | T | 3 | a0003c0007t0009g0041a0003c0007t0010g0007a0003c0007t0010g0042 | 4 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.391+992C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579490 | ||||||
chr4:6579538
|
G | A | 124 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0115others(121): Show | 128 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.391+1040G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579538 | ||||||
chr4:6579542
|
T | TGGTTCTC others(44): Show |
2 | a0003c0070t0002g0034a0022c0069t0003g0033 | 2 | HG02572.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391+1045_391+1046i others(53): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6579542 | |||||
chr4:6579544
|
A | G | 2 | a0003c0070t0002g0034a0022c0069t0003g0033 | 2 | HG02572.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391+1046A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579544 | ||||||
chr4:6579548
|
C | T | 2 | a0003c0070t0002g0034a0022c0069t0003g0033 | 2 | HG02572.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391+1050C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579548 | ||||||
chr4:6579551
|
C | G | 2 | a0003c0070t0002g0034a0022c0069t0003g0033 | 2 | HG02572.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391+1053C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579551 | ||||||
chr4:6579610
|
A | G | 1 | a0003c0070t0002g0034 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.391+1112A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579610 | ||||||
chr4:6579618
|
A | T | 1 | a0001c0001t0001g0322 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.391+1120A>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579618 | ||||||
chr4:6579632
|
C | T | 124 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0115others(121): Show | 128 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.391+1134C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579632 | ||||||
chr4:6579651
|
C | A | 7 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0001g0113others(4): Show | 9 | NA18941.hp2 NA18962.hp2 NA18994.hp1 others(6): Show |
intron_variant | MODIFIER | c.391+1153C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579651 | ||||||
chr4:6579677
|
C | A | 12 | a0001c0003t0002g0202a0002c0004t0002g0208a0002c0004t0003g0196others(9): Show | 12 | HG01255.hp1 HG02109.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.391+1179C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579677 | ||||||
chr4:6579717
|
T | C | 10 | a0001c0055t0002g0122a0002c0002t0009g0037a0003c0007t0009g0041others(7): Show | 11 | HG02258.hp1 HG02258.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.391+1219T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579717 | ||||||
chr4:6579752
|
T | C | 129 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0115others(126): Show | 133 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.391+1254T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579752 | ||||||
chr4:6579778
|
A | G | 6 | a0001c0055t0002g0122a0002c0002t0009g0037a0013c0053t0014g0040others(3): Show | 6 | HG02258.hp1 HG02723.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.391+1280A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579778 | ||||||
chr4:6579834
|
A | G | 125 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0115others(122): Show | 129 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.391+1336A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579834 | ||||||
chr4:6579859
|
G | A | 1 | a0008c0038t0012g0053 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.391+1361G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579859 | ||||||
chr4:6579881
|
T | C | 105 | a0001c0001t0001g0103a0001c0001t0001g0229a0001c0001t0001g0230others(102): Show | 107 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.391+1383T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579881 | ||||||
chr4:6579952
|
C | T | 19 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0117others(16): Show | 21 | HG00423.hp2 HG02071.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.391+1454C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579952 | ||||||
chr4:6579989
|
T | G | 2 | a0024c0067t0025g0031a0025c0068t0001g0032 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.391+1491T>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6579989 | ||||||
chr4:6580005
|
G | A | 145 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0115others(142): Show | 150 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.391+1507G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6580005 | ||||||
chr4:6580114
|
A | G | 124 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0115others(121): Show | 128 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.391+1616A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6580114 | ||||||
chr4:6580161
|
A | G | 124 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0115others(121): Show | 128 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.391+1663A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6580161 | ||||||
chr4:6580210
|
G | A | 11 | a0005c0010t0003g0043a0005c0010t0003g0044a0005c0021t0001g0008others(8): Show | 12 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.391+1712G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6580210 | ||||||
chr4:6580246
|
T | C | 1 | a0002c0002t0002g0085 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.391+1748T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6580246 | ||||||
chr4:6580292
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.391+1794C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6580292 | ||||||
chr4:6580316
|
A | G | 157 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0115others(154): Show | 163 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.391+1818A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6580316 | ||||||
chr4:6580534
|
T | C | 124 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0115others(121): Show | 128 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.391+2036T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6580534 | ||||||
chr4:6580558
|
G | A | 3 | a0003c0007t0009g0041a0003c0007t0010g0007a0003c0007t0010g0042 | 4 | HG02258.hp2 HG02559.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.391+2060G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6580558 | ||||||
chr4:6580631
|
A | T | 2 | a0002c0004t0002g0188a0039c0046t0017g0130 | 2 | HG02647.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.391+2133A>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6580631 | ||||||
chr4:6580750
|
T | C | 146 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0115others(143): Show | 151 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.391+2252T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6580750 | ||||||
chr4:6580752
|
C | T | 2 | a0024c0067t0025g0031a0025c0068t0001g0032 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.391+2254C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6580752 | ||||||
chr4:6580778
|
C | T | 124 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0115others(121): Show | 128 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.391+2280C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6580778 | ||||||
chr4:6580786
|
T | C | 6 | a0001c0055t0002g0122a0002c0002t0009g0037a0013c0053t0014g0040others(3): Show | 6 | HG02258.hp1 HG02723.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.391+2288T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6580786 | ||||||
chr4:6580789
|
C | A | 22 | a0001c0054t0002g0220a0002c0004t0003g0078a0003c0015t0002g0326others(19): Show | 23 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(20): Show |
intron_variant | MODIFIER | c.391+2291C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6580789 | ||||||
chr4:6580806
|
C | G | 4 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+2308C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6580806 | ||||||
chr4:6580823
|
G | A | 3 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328 | 3 | HG02717.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.391+2325G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6580823 | ||||||
chr4:6580879
|
G | A | 2 | a0003c0070t0002g0034a0022c0069t0003g0033 | 2 | HG02572.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391+2381G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6580879 | ||||||
chr4:6580903
|
T | C | 19 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0117others(16): Show | 21 | HG00423.hp2 HG02071.hp1 HG02074.hp1 others(18): Show |
intron_variant | MODIFIER | c.391+2405T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6580903 | ||||||
chr4:6580933
|
G | T | 1 | a0001c0001t0001g0234 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.391+2435G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6580933 | ||||||
chr4:6581018
|
G | T | 2 | a0024c0067t0025g0031a0025c0068t0001g0032 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.391+2520G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6581018 | ||||||
chr4:6581256
|
CT | C | 4 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.391+2759delT | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6581256 | ||||||
chr4:6581265
|
G | A | 18 | a0001c0001t0001g0079a0001c0001t0001g0101a0001c0003t0002g0027others(15): Show | 18 | HG00738.hp2 HG01255.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.391+2767G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6581265 | ||||||
chr4:6581364
|
A | G | 1 | a0001c0001t0001g0305 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.391+2866A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6581364 | ||||||
chr4:6581402
|
G | A | 1 | a0039c0046t0017g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.391+2904G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6581402 | ||||||
chr4:6581420
|
G | A | 1 | a0001c0003t0002g0300 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.391+2922G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6581420 | ||||||
chr4:6581476
|
C | T | 1 | a0002c0002t0001g0023 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.391+2978C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6581476 | ||||||
chr4:6581480
|
G | A | 5 | a0003c0007t0009g0041a0003c0007t0010g0007a0003c0007t0010g0042others(2): Show | 6 | HG02258.hp2 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.391+2982G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6581480 | ||||||
chr4:6581482
|
C | A | 129 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0115others(126): Show | 133 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.391+2984C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6581482 | ||||||
chr4:6581489
|
T | G | 1 | a0001c0001t0001g0022 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.391+2991T>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6581489 | ||||||
chr4:6581572
|
T | C | 1 | a0008c0038t0012g0053 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.391+3074T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6581572 | ||||||
chr4:6581795
|
A | G | 130 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0115others(127): Show | 134 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.391+3297A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6581795 | ||||||
chr4:6581807
|
C | T | 5 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(2): Show | 5 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.391+3309C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6581807 | ||||||
chr4:6581905
|
A | G | 1 | a0001c0001t0001g0322 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.391+3407A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6581905 | ||||||
chr4:6581987
|
C | T | 124 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0115others(121): Show | 128 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.391+3489C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6581987 | ||||||
chr4:6582197
|
C | G | 1 | a0001c0001t0001g0266 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.391+3699C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6582197 | ||||||
chr4:6582285
|
C | T | 1 | a0002c0004t0002g0188 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.391+3787C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6582285 | ||||||
chr4:6582288
|
T | A | 6 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(3): Show | 6 | HG02647.hp2 HG02717.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.391+3790T>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6582288 | ||||||
chr4:6582419
|
A | G | 1 | a0002c0002t0001g0318 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.391+3921A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6582419 | ||||||
chr4:6582425
|
A | G | 2 | a0003c0070t0002g0034a0022c0069t0003g0033 | 2 | HG02572.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.391+3927A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6582425 | ||||||
chr4:6582588
|
C | T | 1 | a0031c0063t0001g0256 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.391+4090C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6582588 | ||||||
chr4:6582652
|
G | A | 7 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(4): Show | 7 | HG01109.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.391+4154G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6582652 | ||||||
chr4:6582687
|
A | T | 3 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328 | 3 | HG02717.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.391+4189A>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6582687 | ||||||
chr4:6582688
|
T | A | 1 | a0001c0001t0001g0165 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.391+4190T>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6582688 | ||||||
chr4:6582713
|
G | A | 1 | a0002c0004t0031g0260 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.391+4215G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6582713 | ||||||
chr4:6582741
|
C | T | 18 | a0001c0054t0002g0220a0002c0004t0003g0078a0005c0010t0003g0043others(15): Show | 19 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.391+4243C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6582741 | ||||||
chr4:6582751
|
A | G | 142 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0115others(139): Show | 147 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.392-4245A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6582751 | ||||||
chr4:6582936
|
A | G | 1 | a0026c0066t0028g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.392-4060A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6582936 | ||||||
chr4:6582942
|
A | G | 1 | a0002c0002t0001g0187 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.392-4054A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6582942 | ||||||
chr4:6583076
|
T | C | 1 | a0044c0026t0001g0141 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.392-3920T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6583076 | ||||||
chr4:6583171
|
AG | A | 6 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(3): Show | 6 | HG02647.hp2 HG02717.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.392-3822delG | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6583171 | |||||
chr4:6583281
|
T | A | 2 | a0005c0010t0003g0010a0038c0045t0002g0082 | 3 | HG02145.hp2 HG02280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.392-3715T>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6583281 | ||||||
chr4:6583378
|
C | G | 5 | a0003c0007t0009g0041a0003c0007t0010g0007a0003c0007t0010g0042others(2): Show | 6 | HG02258.hp2 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.392-3618C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6583378 | ||||||
chr4:6583378
|
CTGGGAGT others(5): Show |
C | 125 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0115others(122): Show | 129 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.392-3615_392-3604d others(14): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6583378 | |||||
chr4:6583397
|
G | A | 1 | a0004c0005t0001g0209 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.392-3599G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6583397 | ||||||
chr4:6583458
|
C | T | 7 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(4): Show | 7 | HG01109.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.392-3538C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6583458 | ||||||
chr4:6583635
|
C | G | 6 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(3): Show | 6 | HG02647.hp2 HG02717.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.392-3361C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6583635 | ||||||
chr4:6583887
|
G | A | 25 | a0001c0001t0001g0009a0001c0001t0001g0064a0001c0001t0001g0065others(22): Show | 28 | HG00609.hp2 HG00621.hp1 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.392-3109G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6583887 | ||||||
chr4:6583896
|
C | G | 1 | a0026c0066t0028g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.392-3100C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6583896 | ||||||
chr4:6584015
|
G | A | 2 | a0005c0010t0003g0043a0005c0010t0003g0044 | 2 | HG02615.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.392-2981G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6584015 | ||||||
chr4:6584093
|
T | C | 277 | a0001c0001t0001g0021a0001c0001t0001g0079a0001c0001t0001g0101others(274): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.392-2903T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6584093 | ||||||
chr4:6584193
|
C | T | 2 | a0002c0004t0003g0078a0041c0042t0007g0077 | 2 | HG02257.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.392-2803C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6584193 | ||||||
chr4:6584221
|
C | T | 2 | a0001c0055t0002g0122a0013c0053t0014g0040 | 2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.392-2775C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6584221 | ||||||
chr4:6584415
|
G | A | 21 | a0001c0001t0001g0107a0001c0001t0001g0115a0001c0001t0001g0117others(18): Show | 23 | HG00423.hp2 HG01261.hp1 HG02071.hp1 others(20): Show |
intron_variant | MODIFIER | c.392-2581G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6584415 | ||||||
chr4:6584715
|
C | T | 27 | a0001c0001t0001g0129a0001c0001t0001g0133a0001c0001t0001g0134others(24): Show | 31 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(28): Show |
intron_variant | MODIFIER | c.392-2281C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6584715 | ||||||
chr4:6584720
|
C | T | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | NA18999.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.392-2276C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6584720 | ||||||
chr4:6584730
|
G | C | 1 | a0028c0048t0001g0120 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.392-2266G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6584730 | ||||||
chr4:6584799
|
G | A | 1 | a0002c0002t0002g0085 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.392-2197G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6584799 | ||||||
chr4:6584854
|
G | T | 3 | a0024c0067t0025g0031a0025c0068t0001g0032a0032c0071t0003g0333 | 3 | HG02258.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.392-2142G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6584854 | ||||||
chr4:6584936
|
G | A | 2 | a0001c0001t0001g0079a0001c0001t0001g0101 | 2 | HG03942.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.392-2060G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6584936 | ||||||
chr4:6584960
|
G | A | 1 | a0002c0004t0002g0214 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.392-2036G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6584960 | ||||||
chr4:6585120
|
C | A | 1 | a0002c0002t0029g0035 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.392-1876C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6585120 | ||||||
chr4:6585123
|
G | A | 2 | a0003c0070t0002g0034a0022c0069t0003g0033 | 2 | HG02572.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.392-1873G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6585123 | ||||||
chr4:6585293
|
G | T | 1 | a0001c0001t0019g0052 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.392-1703G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6585293 | ||||||
chr4:6585582
|
T | A | 1 | a0001c0001t0001g0266 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.392-1414T>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6585582 | ||||||
chr4:6585594
|
G | A | 6 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(3): Show | 6 | HG02647.hp2 HG02717.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.392-1402G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6585594 | ||||||
chr4:6585792
|
G | A | 7 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(4): Show | 7 | HG01109.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.392-1204G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6585792 | ||||||
chr4:6585827
|
A | T | 1 | a0002c0002t0029g0035 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.392-1169A>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6585827 | ||||||
chr4:6585883
|
G | A | 7 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(4): Show | 7 | HG01109.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.392-1113G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6585883 | ||||||
chr4:6586020
|
C | T | 7 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(4): Show | 7 | HG01109.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.392-976C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6586020 | ||||||
chr4:6586051
|
T | C | 1 | a0002c0002t0001g0190 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.392-945T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6586051 | ||||||
chr4:6586052
|
G | GTTTTTTT others(5): Show |
1 | a0026c0066t0028g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.392-944_392-943ins others(12): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6586052 | ||||||
chr4:6586053
|
G | GT | 31 | a0001c0001t0001g0022a0001c0001t0001g0088a0001c0001t0001g0103others(28): Show | 31 | HG00323.hp2 HG00423.hp1 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.392-930dupT | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6586053 | |||||
chr4:6586053
|
G | GTTTTTTT others(20): Show |
2 | a0003c0015t0002g0326a0003c0015t0002g0327 | 2 | HG02717.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.392-930_392-929ins others(27): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6586053 | |||||
chr4:6586053
|
G | GTTTTTTT others(21): Show |
3 | a0003c0015t0002g0328a0011c0009t0016g0026a0039c0046t0017g0130 | 3 | HG02647.hp2 HG02897.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.392-930_392-929ins others(28): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6586053 | |||||
chr4:6586053
|
G | GTTTTTTT others(24): Show |
1 | a0043c0040t0015g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.392-930_392-929ins others(31): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6586053 | |||||
chr4:6586053
|
G | T | 1 | a0026c0066t0028g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.392-943G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6586053 | ||||||
chr4:6586054
|
T | G | 1 | a0001c0003t0002g0162 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.392-942T>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6586054 | ||||||
chr4:6586071
|
C | CA | 7 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(4): Show | 7 | HG01109.hp1 HG02647.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.392-924dupA | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr4 | 6586071 | |||||
chr4:6586112
|
G | A | 1 | a0002c0031t0005g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.392-884G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6586112 | ||||||
chr4:6586232
|
G | A | 1 | a0026c0066t0028g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.392-764G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6586232 | ||||||
chr4:6586512
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.392-484G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6586512 | ||||||
chr4:6586540
|
T | G | 1 | a0001c0003t0003g0228 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.392-456T>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6586540 | ||||||
chr4:6586597
|
C | T | 2 | a0024c0067t0025g0031a0025c0068t0001g0032 | 2 | HG02258.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.392-399C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6586597 | ||||||
chr4:6586641
|
C | G | 1 | a0028c0048t0001g0120 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.392-355C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6586641 | ||||||
chr4:6586642
|
T | A | 1 | a0023c0027t0001g0121 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.392-354T>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6586642 | ||||||
chr4:6586642
|
T | C | 1 | a0028c0048t0001g0120 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.392-354T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6586642 | ||||||
chr4:6586643
|
G | T | 1 | a0028c0048t0001g0120 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.392-353G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 3/18 | chr4 | 6586643 | ||||||
chr4:6587180
|
G | C | 1 | a0008c0038t0012g0053 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.564+12G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6587180 | ||||||
chr4:6587189
|
G | C | 1 | a0001c0003t0002g0054 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.564+21G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6587189 | ||||||
chr4:6587236
|
C | T | 1 | a0011c0009t0032g0084 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.564+68C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6587236 | ||||||
chr4:6587296
|
G | A | 5 | a0005c0010t0003g0043a0005c0010t0003g0044a0005c0021t0001g0008others(2): Show | 6 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.564+128G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6587296 | ||||||
chr4:6587344
|
G | A | 7 | a0001c0055t0002g0122a0002c0002t0009g0037a0008c0038t0012g0053others(4): Show | 7 | HG02258.hp1 HG02723.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.564+176G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6587344 | ||||||
chr4:6587414
|
C | A | 1 | a0002c0002t0029g0035 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.564+246C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6587414 | ||||||
chr4:6587421
|
T | C | 150 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0115others(147): Show | 155 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.564+253T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6587421 | ||||||
chr4:6587567
|
G | T | 3 | a0024c0067t0025g0031a0025c0068t0001g0032a0032c0071t0003g0333 | 3 | HG02258.hp1 HG03209.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.564+399G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6587567 | ||||||
chr4:6587711
|
T | C | 1 | a0002c0002t0001g0176 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.564+543T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6587711 | ||||||
chr4:6587750
|
G | GT | 31 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0147others(28): Show | 37 | HG00140.hp2 HG00639.hp1 HG01109.hp2 others(34): Show |
intron_variant | MODIFIER | c.564+604dupT | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr4 | 6587750 | |||||
chr4:6587750
|
G | GTTTT | 7 | a0001c0001t0001g0117a0002c0002t0004g0110a0022c0069t0003g0033others(4): Show | 7 | HG02258.hp1 HG02647.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.564+601_564+604dup others(4): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr4 | 6587750 | |||||
chr4:6587750
|
G | GTTTTT | 18 | a0001c0001t0001g0107a0002c0002t0001g0051a0002c0002t0001g0062others(15): Show | 18 | HG00423.hp2 HG01109.hp1 HG02071.hp1 others(15): Show |
intron_variant | MODIFIER | c.564+600_564+604dup others(5): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr4 | 6587750 | |||||
chr4:6587750
|
G | GTTTTTT | 6 | a0002c0002t0001g0217a0003c0007t0010g0007a0003c0007t0010g0042others(3): Show | 7 | HG01261.hp1 HG02258.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.564+599_564+604dup others(6): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr4 | 6587750 | |||||
chr4:6587750
|
G | T | 9 | a0001c0001t0001g0331a0002c0002t0001g0017a0002c0002t0001g0173others(6): Show | 9 | NA18944.hp2 NA18948.hp1 NA18952.hp2 others(6): Show |
intron_variant | MODIFIER | c.564+582G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6587750 | ||||||
chr4:6587750
|
GT | G | 8 | a0002c0002t0001g0177a0002c0004t0003g0055a0005c0010t0003g0043others(5): Show | 9 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.564+604delT | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr4 | 6587750 | |||||
chr4:6587750
|
GTTTTTTT others(3): Show |
G | 107 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0229others(104): Show | 109 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.564+595_564+604del others(10): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr4 | 6587750 | |||||
chr4:6587756
|
T | TTTTTG | 6 | a0002c0002t0001g0013a0002c0002t0001g0014a0002c0002t0001g0113others(3): Show | 8 | NA18941.hp2 NA18962.hp2 NA18994.hp1 others(5): Show |
intron_variant | MODIFIER | c.564+592_564+593ins others(5): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr4 | 6587756 | |||||
chr4:6587799
|
G | C | 1 | a0008c0038t0012g0053 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.564+631G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6587799 | ||||||
chr4:6587863
|
T | C | 1 | a0041c0042t0007g0077 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.564+695T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6587863 | ||||||
chr4:6587906
|
C | T | 4 | a0003c0007t0009g0041a0003c0007t0010g0007a0003c0007t0010g0042others(1): Show | 5 | HG02258.hp2 HG02559.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.564+738C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6587906 | ||||||
chr4:6587978
|
C | T | 2 | a0002c0013t0001g0016a0002c0013t0022g0016 | 2 | NA18940.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.564+810C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6587978 | ||||||
chr4:6587988
|
T | TCAC | 3 | a0015c0019t0001g0100a0015c0019t0002g0142a0015c0035t0003g0166 | 3 | HG01243.hp1 HG02451.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.564+821_564+822ins others(3): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | INFO_REALIGN_3_PRIME | chr4 | 6587988 | |||||
chr4:6588209
|
A | G | 1 | a0002c0002t0001g0175 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.565-836A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6588209 | ||||||
chr4:6588283
|
G | A | 131 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0115others(128): Show | 135 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.565-762G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6588283 | ||||||
chr4:6588290
|
C | T | 1 | a0002c0002t0029g0035 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.565-755C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6588290 | ||||||
chr4:6588485
|
T | C | 6 | a0005c0010t0003g0043a0005c0010t0003g0044a0005c0021t0001g0008others(3): Show | 7 | HG01891.hp2 HG02257.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.565-560T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6588485 | ||||||
chr4:6588521
|
C | G | 4 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.565-524C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6588521 | ||||||
chr4:6588578
|
G | T | 1 | a0002c0004t0002g0161 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.565-467G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6588578 | ||||||
chr4:6588622
|
G | A | 4 | a0024c0067t0025g0031a0025c0068t0001g0032a0026c0066t0028g0131others(1): Show | 4 | HG01109.hp1 HG02258.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.565-423G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6588622 | ||||||
chr4:6588663
|
T | C | 159 | a0001c0001t0001g0103a0001c0001t0001g0107a0001c0001t0001g0115others(156): Show | 165 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(162): Show |
intron_variant | MODIFIER | c.565-382T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6588663 | ||||||
chr4:6588850
|
G | A | 1 | a0041c0042t0007g0077 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.565-195G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6588850 | ||||||
chr4:6588868
|
C | T | 1 | a0002c0002t0001g0172 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.565-177C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6588868 | ||||||
chr4:6588869
|
G | A | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG00438.hp2 HG00673.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.565-176G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6588869 | ||||||
chr4:6588899
|
G | A | 2 | a0002c0004t0003g0055a0002c0004t0003g0056 | 2 | HG02486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.565-146G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6588899 | ||||||
chr4:6588906
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.565-139G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6588906 | ||||||
chr4:6588946
|
A | G | 1 | a0001c0003t0002g0072 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.565-99A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6588946 | ||||||
chr4:6588948
|
G | T | 1 | a0001c0003t0002g0072 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.565-97G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6588948 | ||||||
chr4:6588949
|
T | G | 1 | a0001c0003t0002g0072 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.565-96T>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6588949 | ||||||
chr4:6588972
|
G | T | 1 | a0002c0004t0002g0198 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.565-73G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 4/18 | chr4 | 6588972 | ||||||
chr4:6589174
|
C | T | 11 | a0003c0007t0009g0041a0003c0007t0010g0007a0003c0007t0010g0042others(8): Show | 13 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.680+14C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6589174 | ||||||
chr4:6589288
|
C | T | 126 | a0001c0001t0001g0103a0001c0001t0001g0115a0001c0001t0001g0133others(123): Show | 130 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.680+128C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6589288 | ||||||
chr4:6589392
|
C | G | 1 | a0013c0052t0003g0225 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.680+232C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6589392 | ||||||
chr4:6589533
|
G | A | 1 | a0013c0051t0001g0223 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.680+373G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6589533 | ||||||
chr4:6589767
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.680+607C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6589767 | ||||||
chr4:6589982
|
G | A | 1 | a0003c0070t0002g0034 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.680+822G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6589982 | ||||||
chr4:6590007
|
C | G | 3 | a0001c0003t0002g0300a0006c0016t0003g0271a0012c0022t0001g0315 | 3 | HG02602.hp2 HG03017.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.680+847C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6590007 | ||||||
chr4:6590200
|
C | T | 292 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(289): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.680+1040C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6590200 | ||||||
chr4:6590309
|
C | G | 1 | a0002c0002t0001g0301 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.680+1149C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6590309 | ||||||
chr4:6590334
|
A | G | 299 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(296): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.680+1174A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6590334 | ||||||
chr4:6590466
|
C | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0134 | 2 | HG00099.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.680+1306C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6590466 | ||||||
chr4:6590478
|
C | T | 114 | a0001c0001t0001g0079a0001c0001t0001g0101a0001c0001t0001g0103others(111): Show | 116 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.680+1318C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6590478 | ||||||
chr4:6590555
|
G | A | 1 | a0002c0002t0001g0178 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.680+1395G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6590555 | ||||||
chr4:6590574
|
A | T | 8 | a0002c0004t0002g0208a0002c0004t0003g0196a0002c0004t0003g0203others(5): Show | 8 | HG01255.hp1 HG02109.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.680+1414A>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6590574 | ||||||
chr4:6590622
|
C | T | 1 | a0008c0038t0012g0053 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.680+1462C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6590622 | ||||||
chr4:6590647
|
G | A | 1 | a0002c0002t0001g0023 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.680+1487G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6590647 | ||||||
chr4:6590744
|
C | T | 1 | a0003c0070t0002g0034 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.680+1584C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6590744 | ||||||
chr4:6590749
|
G | A | 12 | a0001c0003t0002g0027a0002c0004t0002g0208a0002c0004t0003g0196others(9): Show | 12 | HG00733.hp1 HG01255.hp1 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.680+1589G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6590749 | ||||||
chr4:6590860
|
C | T | 1 | a0003c0070t0002g0034 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.680+1700C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6590860 | ||||||
chr4:6590989
|
A | C | 1 | a0001c0001t0001g0253 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.680+1829A>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6590989 | ||||||
chr4:6591038
|
C | T | 1 | a0002c0002t0002g0123 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.680+1878C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6591038 | ||||||
chr4:6591128
|
A | G | 1 | a0002c0002t0001g0216 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.680+1968A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6591128 | ||||||
chr4:6591149
|
A | G | 1 | a0003c0007t0010g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.680+1989A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6591149 | ||||||
chr4:6591390
|
T | C | 133 | a0001c0001t0001g0079a0001c0001t0001g0101a0001c0001t0001g0103others(130): Show | 136 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.681-1783T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6591390 | ||||||
chr4:6591472
|
C | T | 110 | a0001c0001t0001g0079a0001c0001t0001g0101a0001c0001t0001g0103others(107): Show | 111 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.681-1701C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6591472 | ||||||
chr4:6591527
|
G | C | 1 | a0008c0038t0012g0053 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.681-1646G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6591527 | ||||||
chr4:6591710
|
G | A | 116 | a0001c0001t0001g0021a0001c0001t0001g0147a0001c0001t0001g0149others(113): Show | 126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.681-1463G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6591710 | ||||||
chr4:6592053
|
C | T | 1 | a0003c0044t0002g0132 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.681-1120C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6592053 | ||||||
chr4:6592282
|
A | C | 1 | a0041c0042t0007g0077 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.681-891A>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6592282 | ||||||
chr4:6592445
|
C | G | 1 | a0041c0042t0007g0077 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.681-728C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6592445 | ||||||
chr4:6592446
|
T | A | 10 | a0001c0054t0002g0220a0003c0036t0002g0036a0003c0070t0002g0034others(7): Show | 10 | HG02258.hp1 HG02451.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.681-727T>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6592446 | ||||||
chr4:6592462
|
T | C | 1 | a0001c0001t0001g0322 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.681-711T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6592462 | ||||||
chr4:6592504
|
G | A | 3 | a0009c0011t0001g0046a0009c0011t0001g0105a0009c0011t0002g0104 | 3 | HG03130.hp1 HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.681-669G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6592504 | ||||||
chr4:6592508
|
C | G | 1 | a0001c0001t0001g0234 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.681-665C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6592508 | ||||||
chr4:6592529
|
G | A | 157 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(154): Show | 160 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.681-644G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6592529 | ||||||
chr4:6592568
|
C | A | 174 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238others(171): Show | 193 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.681-605C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6592568 | ||||||
chr4:6592685
|
G | A | 5 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(2): Show | 5 | HG00099.hp1 HG01433.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.681-488G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6592685 | ||||||
chr4:6592805
|
T | C | 1 | a0002c0002t0029g0035 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.681-368T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6592805 | ||||||
chr4:6592817
|
G | GT | 17 | a0001c0003t0002g0071a0001c0054t0002g0220a0001c0055t0002g0122others(14): Show | 18 | HG02258.hp1 HG02258.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.681-350dupT | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr4 | 6592817 | |||||
chr4:6592942
|
C | G | 152 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(149): Show | 155 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.681-231C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6592942 | ||||||
chr4:6592970
|
C | T | 2 | a0001c0055t0002g0122a0013c0053t0014g0040 | 2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.681-203C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6592970 | ||||||
chr4:6593100
|
A | G | 317 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(314): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.681-73A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6593100 | ||||||
chr4:6593389
|
C | T | 7 | a0005c0010t0003g0010a0005c0010t0003g0043a0005c0010t0003g0044others(4): Show | 8 | HG02145.hp2 HG02280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.858+39C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 6/18 | chr4 | 6593389 | ||||||
chr4:6593488
|
C | T | 1 | a0001c0001t0001g0060 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.858+138C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 6/18 | chr4 | 6593488 | ||||||
chr4:6593607
|
G | GC | 3 | a0002c0002t0001g0013a0002c0002t0001g0114a0002c0004t0002g0112 | 4 | NA18994.hp1 NA19000.hp1 NA19065.hp2 others(1): Show |
intron_variant | MODIFIER | c.858+258dupC | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 6593607 | |||||
chr4:6593627
|
G | A | 2 | a0001c0001t0001g0239a0001c0001t0001g0240 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.858+277G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 6/18 | chr4 | 6593627 | ||||||
chr4:6593651
|
A | C | 152 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(149): Show | 155 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.858+301A>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 6/18 | chr4 | 6593651 | ||||||
chr4:6593664
|
G | A | 1 | a0002c0004t0003g0078 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.858+314G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 6/18 | chr4 | 6593664 | ||||||
chr4:6593715
|
C | A | 1 | a0001c0055t0002g0122 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.858+365C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 6/18 | chr4 | 6593715 | ||||||
chr4:6593742
|
G | A | 1 | a0001c0001t0001g0234 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.858+392G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 6/18 | chr4 | 6593742 | ||||||
chr4:6593753
|
C | A | 2 | a0002c0002t0001g0087a0002c0002t0001g0250 | 2 | HG02055.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.858+403C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 6/18 | chr4 | 6593753 | ||||||
chr4:6593951
|
G | T | 3 | a0001c0001t0001g0296a0001c0001t0001g0297a0001c0001t0001g0298 | 3 | HG00438.hp2 HG00673.hp1 NA18957.hp1 |
intron_variant | MODIFIER | c.859-583G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 6/18 | chr4 | 6593951 | ||||||
chr4:6594019
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.859-515G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 6/18 | chr4 | 6594019 | ||||||
chr4:6594307
|
GTGGCGCC others(17): Show |
G | 173 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(170): Show | 178 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.859-224_859-201del others(24): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr4 | 6594307 | |||||
chr4:6594314
|
C | A | 1 | a0026c0066t0028g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.859-220C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 6/18 | chr4 | 6594314 | ||||||
chr4:6594364
|
G | A | 4 | a0011c0009t0002g0048a0011c0009t0002g0222a0011c0009t0016g0026others(1): Show | 4 | HG02723.hp2 HG02818.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.859-170G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 6/18 | chr4 | 6594364 | ||||||
chr4:6594426
|
C | T | 1 | a0003c0007t0009g0041 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.859-108C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 6/18 | chr4 | 6594426 | ||||||
chr4:6594468
|
G | A | 8 | a0005c0010t0003g0010a0005c0010t0003g0043a0005c0010t0003g0044others(5): Show | 10 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.859-66G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 6/18 | chr4 | 6594468 | ||||||
chr4:6594749
|
G | A | 102 | a0001c0001t0001g0021a0001c0001t0001g0079a0001c0001t0001g0095others(99): Show | 102 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.1057+17G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6594749 | ||||||
chr4:6594750
|
C | T | 1 | a0003c0044t0002g0132 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1057+18C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6594750 | ||||||
chr4:6594788
|
C | T | 331 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(328): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1057+56C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6594788 | ||||||
chr4:6594790
|
T | C | 5 | a0002c0004t0003g0203a0002c0004t0003g0323a0009c0028t0003g0047others(2): Show | 5 | HG02109.hp2 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1057+58T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6594790 | ||||||
chr4:6594825
|
C | T | 145 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(142): Show | 161 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1057+93C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6594825 | ||||||
chr4:6594836
|
C | G | 2 | a0001c0001t0001g0292a0001c0003t0002g0291 | 2 | NA18964.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.1057+104C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6594836 | ||||||
chr4:6594920
|
A | G | 178 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(175): Show | 184 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.1057+188A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6594920 | ||||||
chr4:6595077
|
C | T | 3 | a0003c0041t0002g0076a0021c0020t0002g0049a0042c0043t0030g0089 | 3 | HG01884.hp1 HG01884.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.1057+345C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6595077 | ||||||
chr4:6595087
|
C | T | 3 | a0009c0011t0001g0046a0009c0011t0001g0105a0009c0011t0002g0104 | 3 | HG03130.hp1 HG03139.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1057+355C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6595087 | ||||||
chr4:6595236
|
C | A | 1 | a0002c0004t0003g0206 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1057+504C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6595236 | ||||||
chr4:6595362
|
C | T | 101 | a0001c0001t0001g0021a0001c0001t0001g0079a0001c0001t0001g0095others(98): Show | 101 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.1057+630C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6595362 | ||||||
chr4:6595395
|
A | C | 331 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(328): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.1057+663A>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6595395 | ||||||
chr4:6595481
|
G | A | 1 | a0002c0002t0002g0325 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1057+749G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6595481 | ||||||
chr4:6595553
|
T | G | 152 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(149): Show | 155 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.1057+821T>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6595553 | ||||||
chr4:6595726
|
A | T | 1 | a0001c0001t0001g0286 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1057+994A>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6595726 | ||||||
chr4:6595861
|
C | T | 1 | a0002c0002t0001g0106 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1057+1129C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6595861 | ||||||
chr4:6595901
|
C | T | 2 | a0016c0014t0006g0200a0016c0014t0006g0201 | 2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1057+1169C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6595901 | ||||||
chr4:6595910
|
C | G | 1 | a0041c0042t0007g0077 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1057+1178C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6595910 | ||||||
chr4:6596091
|
G | A | 1 | a0012c0022t0001g0247 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1058-1022G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6596091 | ||||||
chr4:6596109
|
CTGTCCAG others(10): Show |
C | 1 | a0003c0070t0002g0034 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1058-985_1058-969d others(19): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 6596109 | |||||
chr4:6596128
|
GTCCAGGT others(10): Show |
G | 2 | a0001c0054t0002g0220a0002c0002t0001g0091 | 2 | HG02895.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1058-961_1058-945d others(19): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 6596128 | |||||
chr4:6596139
|
C | T | 166 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(163): Show | 171 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.1058-974C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6596139 | ||||||
chr4:6596145
|
A | ATCCAGGT others(37): Show |
5 | a0002c0004t0003g0203a0002c0004t0003g0323a0009c0028t0003g0047others(2): Show | 5 | HG02109.hp2 HG02809.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058-940_1058-897d others(46): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 6596145 | |||||
chr4:6596166
|
A | G | 160 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(157): Show | 163 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.1058-947A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6596166 | ||||||
chr4:6596176
|
GGGTGGGC others(10): Show |
G | 10 | a0003c0036t0002g0036a0005c0010t0003g0010a0005c0010t0003g0043others(7): Show | 12 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1058-925_1058-909d others(19): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | INFO_REALIGN_3_PRIME | chr4 | 6596176 | |||||
chr4:6596188
|
C | T | 130 | a0002c0002t0001g0001a0002c0002t0001g0003a0002c0002t0001g0004others(127): Show | 146 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.1058-925C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6596188 | ||||||
chr4:6596226
|
G | C | 1 | a0014c0012t0002g0197 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1058-887G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6596226 | ||||||
chr4:6596441
|
G | A | 2 | a0001c0055t0002g0122a0013c0053t0014g0040 | 2 | HG02723.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.1058-672G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6596441 | ||||||
chr4:6596457
|
A | G | 179 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(176): Show | 185 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1058-656A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6596457 | ||||||
chr4:6596623
|
C | G | 25 | a0001c0055t0002g0122a0003c0007t0009g0041a0003c0007t0010g0007others(22): Show | 28 | HG00733.hp1 HG01243.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.1058-490C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6596623 | ||||||
chr4:6596652
|
G | C | 10 | a0003c0036t0002g0036a0005c0010t0003g0010a0005c0010t0003g0043others(7): Show | 12 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1058-461G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6596652 | ||||||
chr4:6596789
|
T | C | 1 | a0001c0003t0002g0300 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1058-324T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6596789 | ||||||
chr4:6596956
|
G | T | 2 | a0002c0002t0001g0091a0002c0002t0001g0171 | 2 | NA18959.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.1058-157G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6596956 | ||||||
chr4:6596973
|
T | C | 17 | a0001c0055t0002g0122a0003c0007t0009g0041a0003c0007t0010g0007others(14): Show | 20 | HG00733.hp1 HG01891.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1058-140T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6596973 | ||||||
chr4:6597068
|
C | T | 1 | a0034c0056t0007g0221 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1058-45C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6597068 | ||||||
chr4:6597077
|
G | C | 1 | a0002c0002t0001g0150 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1058-36G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 7/18 | chr4 | 6597077 | ||||||
chr4:6597566
|
C | T | 6 | a0005c0010t0003g0010a0005c0010t0003g0043a0005c0010t0003g0044others(3): Show | 8 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1248+263C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 8/18 | chr4 | 6597566 | ||||||
chr4:6597567
|
A | C | 1 | a0035c0029t0001g0140 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1248+264A>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 8/18 | chr4 | 6597567 | ||||||
chr4:6597575
|
C | G | 8 | a0005c0010t0003g0010a0005c0010t0003g0043a0005c0010t0003g0044others(5): Show | 10 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1248+272C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 8/18 | chr4 | 6597575 | ||||||
chr4:6597735
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1248+432C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 8/18 | chr4 | 6597735 | ||||||
chr4:6597828
|
G | A | 9 | a0003c0036t0002g0036a0005c0010t0003g0010a0005c0010t0003g0043others(6): Show | 11 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1249-370G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 8/18 | chr4 | 6597828 | ||||||
chr4:6597901
|
G | C | 1 | a0001c0001t0001g0229 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1249-297G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 8/18 | chr4 | 6597901 | ||||||
chr4:6597957
|
T | A | 178 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(175): Show | 184 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.1249-241T>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 8/18 | chr4 | 6597957 | ||||||
chr4:6597988
|
A | G | 28 | a0001c0054t0002g0220a0001c0055t0002g0122a0003c0015t0002g0326others(25): Show | 30 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.1249-210A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 8/18 | chr4 | 6597988 | ||||||
chr4:6598118
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1249-80G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 8/18 | chr4 | 6598118 | ||||||
chr4:6598378
|
C | T | 1 | a0026c0066t0028g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1405+24C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6598378 | ||||||
chr4:6598387
|
C | G | 1 | a0006c0050t0026g0224 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1405+33C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6598387 | ||||||
chr4:6598395
|
AG | A | 6 | a0001c0001t0001g0009a0001c0001t0001g0065a0001c0003t0002g0002others(3): Show | 9 | HG00609.hp2 NA18942.hp1 NA18969.hp2 others(6): Show |
intron_variant | MODIFIER | c.1405+44delG | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr4 | 6598395 | |||||
chr4:6598400
|
G | A | 1 | a0007c0006t0001g0059 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1405+46G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6598400 | ||||||
chr4:6598460
|
C | T | 1 | a0002c0002t0033g0158 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1405+106C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6598460 | ||||||
chr4:6598470
|
G | A | 6 | a0001c0055t0002g0122a0003c0015t0002g0326a0003c0015t0002g0327others(3): Show | 6 | HG02717.hp2 HG02723.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1405+116G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6598470 | ||||||
chr4:6598479
|
C | T | 2 | a0003c0041t0002g0076a0042c0043t0030g0089 | 2 | HG01884.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.1405+125C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6598479 | ||||||
chr4:6598513
|
C | A | 13 | a0001c0054t0002g0220a0003c0041t0002g0076a0003c0070t0002g0034others(10): Show | 13 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1405+159C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6598513 | ||||||
chr4:6598705
|
C | T | 1 | a0021c0020t0002g0049 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1405+351C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6598705 | ||||||
chr4:6598738
|
C | T | 2 | a0001c0001t0001g0303a0029c0059t0001g0304 | 2 | NA18977.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1405+384C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6598738 | ||||||
chr4:6598795
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1405+441C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6598795 | ||||||
chr4:6598824
|
C | T | 4 | a0003c0015t0002g0326a0003c0015t0002g0327a0003c0015t0002g0328others(1): Show | 4 | HG02717.hp2 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1405+470C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6598824 | ||||||
chr4:6598868
|
G | A | 1 | a0001c0003t0002g0162 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1405+514G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6598868 | ||||||
chr4:6598983
|
G | A | 1 | a0026c0066t0028g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1405+629G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6598983 | ||||||
chr4:6599165
|
A | T | 20 | a0001c0054t0002g0220a0001c0055t0002g0122a0003c0015t0002g0326others(17): Show | 20 | HG01243.hp1 HG01884.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1405+811A>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6599165 | ||||||
chr4:6599278
|
A | AT | 17 | a0003c0036t0002g0036a0005c0010t0003g0010a0005c0010t0003g0043others(14): Show | 19 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.1405+932dupT | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr4 | 6599278 | |||||
chr4:6599537
|
G | A | 7 | a0001c0055t0002g0122a0003c0015t0002g0326a0003c0015t0002g0327others(4): Show | 7 | HG01884.hp2 HG02717.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.1406-1086G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6599537 | ||||||
chr4:6599579
|
C | G | 21 | a0003c0007t0009g0041a0003c0007t0010g0007a0003c0007t0010g0042others(18): Show | 24 | HG00733.hp1 HG01891.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.1406-1044C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6599579 | ||||||
chr4:6599588
|
A | G | 42 | a0001c0054t0002g0220a0001c0055t0002g0122a0003c0007t0009g0041others(39): Show | 45 | HG00733.hp1 HG01243.hp1 HG01884.hp1 others(42): Show |
intron_variant | MODIFIER | c.1406-1035A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6599588 | ||||||
chr4:6599594
|
C | A | 19 | a0001c0054t0002g0220a0001c0055t0002g0122a0003c0015t0002g0326others(16): Show | 19 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1406-1029C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6599594 | ||||||
chr4:6599594
|
C | T | 9 | a0003c0036t0002g0036a0005c0010t0003g0010a0005c0010t0003g0043others(6): Show | 11 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1406-1029C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6599594 | ||||||
chr4:6599604
|
A | G | 1 | a0042c0043t0030g0089 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1406-1019A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6599604 | ||||||
chr4:6599611
|
C | T | 19 | a0001c0054t0002g0220a0001c0055t0002g0122a0003c0015t0002g0326others(16): Show | 19 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.1406-1012C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6599611 | ||||||
chr4:6599650
|
G | A | 1 | a0042c0043t0030g0089 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1406-973G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6599650 | ||||||
chr4:6599662
|
C | CA | 10 | a0001c0003t0002g0027a0001c0003t0002g0320a0002c0002t0001g0144others(7): Show | 10 | HG01884.hp1 HG01891.hp1 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.1406-940dupA | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr4 | 6599662 | |||||
chr4:6599662
|
CA | C | 141 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(138): Show | 145 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1406-940delA | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr4 | 6599662 | |||||
chr4:6599662
|
CAA | C | 9 | a0001c0001t0004g0278a0001c0003t0002g0066a0001c0003t0002g0233others(6): Show | 9 | HG01884.hp2 HG02717.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1406-941_1406-940d others(4): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | INFO_REALIGN_3_PRIME | chr4 | 6599662 | |||||
chr4:6599694
|
C | G | 1 | a0042c0043t0030g0089 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1406-929C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6599694 | ||||||
chr4:6599757
|
C | T | 1 | a0001c0001t0001g0329 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1406-866C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6599757 | ||||||
chr4:6599887
|
G | A | 12 | a0001c0054t0002g0220a0003c0070t0002g0034a0006c0050t0026g0224others(9): Show | 12 | HG01243.hp1 HG01891.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1406-736G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6599887 | ||||||
chr4:6599957
|
ACACAGGA others(3): Show |
A | 2 | a0002c0002t0001g0051a0002c0002t0001g0106 | 2 | HG02071.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1406-665_1406-656d others(12): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6599957 | ||||||
chr4:6600015
|
A | G | 186 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(183): Show | 192 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.1406-608A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6600015 | ||||||
chr4:6600146
|
G | A | 1 | a0001c0003t0002g0027 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1406-477G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6600146 | ||||||
chr4:6600161
|
A | G | 162 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(159): Show | 165 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.1406-462A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6600161 | ||||||
chr4:6600194
|
C | G | 1 | a0013c0052t0003g0225 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1406-429C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6600194 | ||||||
chr4:6600251
|
C | G | 185 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(182): Show | 191 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.1406-372C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6600251 | ||||||
chr4:6600397
|
C | T | 6 | a0003c0007t0009g0041a0003c0007t0010g0007a0003c0007t0010g0042others(3): Show | 7 | HG00733.hp1 HG02257.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1406-226C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6600397 | ||||||
chr4:6600410
|
C | G | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0238 | 3 | HG01496.hp1 HG02273.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.1406-213C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6600410 | ||||||
chr4:6600443
|
A | G | 1 | a0001c0001t0001g0322 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1406-180A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6600443 | ||||||
chr4:6600466
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1406-157A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6600466 | ||||||
chr4:6600514
|
G | T | 1 | a0001c0001t0001g0299 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1406-109G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6600514 | ||||||
chr4:6600528
|
A | G | 185 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(182): Show | 191 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.1406-95A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6600528 | ||||||
chr4:6600556
|
G | T | 1 | a0025c0068t0001g0032 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1406-67G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 9/18 | chr4 | 6600556 | ||||||
chr4:6600789
|
A | G | 185 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(182): Show | 191 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.1539+33A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6600789 | ||||||
chr4:6600829
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1539+73C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6600829 | ||||||
chr4:6600921
|
C | T | 41 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(38): Show | 44 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.1539+165C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6600921 | ||||||
chr4:6600970
|
T | C | 1 | a0002c0002t0001g0181 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1539+214T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6600970 | ||||||
chr4:6601138
|
A | C | 5 | a0011c0009t0002g0048a0011c0009t0016g0026a0011c0009t0032g0084others(2): Show | 5 | HG02280.hp2 HG02622.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1539+382A>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6601138 | ||||||
chr4:6601214
|
T | G | 314 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(311): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.1539+458T>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6601214 | ||||||
chr4:6601326
|
A | G | 3 | a0001c0001t0001g0285a0001c0001t0001g0330a0001c0001t0018g0284 | 3 | HG00642.hp1 HG01361.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1539+570A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6601326 | ||||||
chr4:6601333
|
G | A | 2 | a0037c0047t0027g0195a0040c0039t0007g0050 | 2 | HG02280.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1539+577G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6601333 | ||||||
chr4:6601358
|
A | C | 1 | a0001c0003t0002g0071 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1539+602A>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6601358 | ||||||
chr4:6601398
|
G | T | 1 | a0002c0002t0001g0171 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1539+642G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6601398 | ||||||
chr4:6601414
|
C | T | 1 | a0001c0001t0001g0263 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1539+658C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6601414 | ||||||
chr4:6601500
|
C | CA | 30 | a0001c0003t0002g0058a0001c0054t0002g0220a0002c0032t0011g0024others(27): Show | 33 | HG00733.hp1 HG01891.hp1 HG01891.hp2 others(30): Show |
intron_variant | MODIFIER | c.1539+760dupA | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 6601500 | |||||
chr4:6601500
|
CA | C | 7 | a0001c0001t0001g0235a0001c0001t0001g0240a0001c0001t0004g0278others(4): Show | 7 | HG01167.hp1 HG01256.hp1 NA18953.hp2 others(4): Show |
intron_variant | MODIFIER | c.1539+760delA | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 6601500 | |||||
chr4:6601564
|
A | AAGCAGGG | 98 | a0001c0001t0001g0021a0001c0001t0001g0079a0001c0001t0001g0095others(95): Show | 98 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.1539+811_1539+817d others(9): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 6601564 | |||||
chr4:6601606
|
G | A | 14 | a0005c0010t0003g0010a0005c0010t0003g0043a0005c0010t0003g0044others(11): Show | 16 | HG01891.hp2 HG02145.hp2 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.1539+850G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6601606 | ||||||
chr4:6601923
|
G | C | 1 | a0002c0002t0001g0019 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1539+1167G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6601923 | ||||||
chr4:6602017
|
C | T | 1 | a0008c0038t0012g0053 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1539+1261C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6602017 | ||||||
chr4:6602236
|
C | A | 1 | a0022c0037t0003g0124 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1539+1480C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6602236 | ||||||
chr4:6602388
|
C | T | 1 | a0001c0003t0002g0162 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1539+1632C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6602388 | ||||||
chr4:6602421
|
G | A | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1539+1665G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6602421 | ||||||
chr4:6602670
|
C | CT | 53 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(50): Show | 56 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.1539+1931dupT | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr4 | 6602670 | |||||
chr4:6602790
|
T | C | 184 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(181): Show | 190 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.1539+2034T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6602790 | ||||||
chr4:6602829
|
C | T | 7 | a0003c0036t0002g0036a0003c0070t0002g0034a0016c0014t0006g0199others(4): Show | 7 | HG02572.hp2 HG03041.hp1 HG03130.hp2 others(4): Show |
intron_variant | MODIFIER | c.1539+2073C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6602829 | ||||||
chr4:6602956
|
A | G | 184 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(181): Show | 190 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.1540-2099A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6602956 | ||||||
chr4:6603023
|
G | A | 3 | a0001c0001t0001g0285a0001c0001t0001g0330a0001c0001t0018g0284 | 3 | HG00642.hp1 HG01361.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1540-2032G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6603023 | ||||||
chr4:6603123
|
G | A | 23 | a0001c0054t0002g0220a0003c0007t0009g0041a0003c0007t0010g0007others(20): Show | 26 | HG00733.hp1 HG01884.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1540-1932G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6603123 | ||||||
chr4:6603277
|
C | T | 180 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(177): Show | 186 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1540-1778C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6603277 | ||||||
chr4:6603279
|
G | T | 1 | a0001c0003t0002g0027 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1540-1776G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6603279 | ||||||
chr4:6603377
|
G | C | 1 | a0007c0006t0001g0159 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1540-1678G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6603377 | ||||||
chr4:6603544
|
C | T | 4 | a0008c0038t0012g0053a0021c0020t0002g0049a0026c0066t0028g0131others(1): Show | 4 | HG01109.hp1 HG02257.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1540-1511C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6603544 | ||||||
chr4:6603567
|
C | T | 1 | a0016c0014t0006g0201 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1540-1488C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6603567 | ||||||
chr4:6603568
|
G | A | 1 | a0039c0046t0017g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1540-1487G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6603568 | ||||||
chr4:6603568
|
G | T | 1 | a0022c0037t0003g0124 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1540-1487G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6603568 | ||||||
chr4:6603635
|
G | A | 5 | a0003c0007t0009g0041a0003c0007t0010g0007a0003c0007t0010g0042others(2): Show | 6 | HG00733.hp1 HG02258.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1540-1420G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6603635 | ||||||
chr4:6603830
|
A | G | 1 | a0011c0009t0002g0048 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1540-1225A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6603830 | ||||||
chr4:6603859
|
A | G | 322 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(319): Show | 344 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(341): Show |
intron_variant | MODIFIER | c.1540-1196A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6603859 | ||||||
chr4:6603991
|
T | C | 312 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(309): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1540-1064T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6603991 | ||||||
chr4:6604104
|
G | A | 2 | a0002c0002t0001g0169a0002c0004t0002g0161 | 2 | HG01934.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1540-951G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6604104 | ||||||
chr4:6604104
|
G | C | 1 | a0001c0003t0002g0162 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1540-951G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6604104 | ||||||
chr4:6604289
|
G | A | 1 | a0001c0003t0002g0202 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1540-766G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6604289 | ||||||
chr4:6604292
|
T | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | NA18999.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.1540-763T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6604292 | ||||||
chr4:6604398
|
G | A | 1 | a0001c0001t0001g0299 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1540-657G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6604398 | ||||||
chr4:6604458
|
G | A | 1 | a0001c0003t0002g0202 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1540-597G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6604458 | ||||||
chr4:6604524
|
G | T | 104 | a0001c0001t0001g0021a0001c0001t0001g0079a0001c0001t0001g0095others(101): Show | 104 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1540-531G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6604524 | ||||||
chr4:6604542
|
G | A | 1 | a0002c0004t0002g0188 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1540-513G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6604542 | ||||||
chr4:6604615
|
G | T | 1 | a0001c0054t0002g0220 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1540-440G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6604615 | ||||||
chr4:6604626
|
G | A | 2 | a0001c0054t0002g0220a0034c0056t0007g0221 | 2 | HG02895.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1540-429G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6604626 | ||||||
chr4:6604701
|
G | C | 7 | a0002c0002t0001g0051a0002c0002t0001g0106a0002c0002t0001g0108others(4): Show | 7 | HG00423.hp2 HG02071.hp1 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.1540-354G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6604701 | ||||||
chr4:6604785
|
G | T | 41 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(38): Show | 44 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(41): Show |
intron_variant | MODIFIER | c.1540-270G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6604785 | ||||||
chr4:6604878
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1540-177A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6604878 | ||||||
chr4:6604944
|
G | A | 1 | a0013c0053t0014g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1540-111G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6604944 | ||||||
chr4:6605366
|
A | G | 1 | a0040c0039t0007g0050 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1814+37A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6605366 | ||||||
chr4:6605444
|
G | A | 6 | a0005c0010t0003g0010a0005c0010t0003g0043a0005c0010t0003g0044others(3): Show | 8 | HG01891.hp2 HG02280.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1814+115G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6605444 | ||||||
chr4:6605568
|
A | G | 51 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(48): Show | 54 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.1814+239A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6605568 | ||||||
chr4:6605668
|
C | G | 3 | a0002c0002t0001g0332a0020c0018t0001g0020a0020c0018t0021g0020 | 3 | NA18944.hp2 NA18952.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1814+339C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6605668 | ||||||
chr4:6605669
|
G | A | 1 | a0003c0044t0002g0132 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1814+340G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6605669 | ||||||
chr4:6605705
|
T | C | 1 | a0002c0002t0002g0325 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1814+376T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6605705 | ||||||
chr4:6605733
|
C | T | 173 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(170): Show | 179 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.1814+404C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6605733 | ||||||
chr4:6605746
|
A | G | 2 | a0001c0001t0001g0252a0001c0001t0001g0297 | 2 | HG00438.hp2 NA18990.hp1 |
intron_variant | MODIFIER | c.1814+417A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6605746 | ||||||
chr4:6605911
|
C | T | 2 | a0001c0055t0002g0122a0003c0041t0002g0076 | 2 | HG01884.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1814+582C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6605911 | ||||||
chr4:6605911
|
CCATT | C | 169 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(166): Show | 175 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.1814+606_1814+609d others(6): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | INFO_REALIGN_3_PRIME | chr4 | 6605911 | |||||
chr4:6606103
|
T | C | 74 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(71): Show | 81 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(78): Show |
intron_variant | MODIFIER | c.1814+774T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6606103 | ||||||
chr4:6606131
|
G | A | 1 | a0002c0002t0024g0184 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1814+802G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6606131 | ||||||
chr4:6606351
|
G | A | 2 | a0007c0006t0001g0059a0007c0006t0001g0080 | 2 | HG01361.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.1814+1022G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6606351 | ||||||
chr4:6606367
|
T | A | 1 | a0001c0001t0004g0310 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1814+1038T>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6606367 | ||||||
chr4:6606390
|
T | C | 1 | a0005c0021t0001g0008 | 2 | HG01891.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1814+1061T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6606390 | ||||||
chr4:6606442
|
C | T | 33 | a0002c0002t0001g0003a0002c0002t0001g0004a0002c0002t0001g0028others(30): Show | 37 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.1814+1113C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6606442 | ||||||
chr4:6606478
|
G | A | 1 | a0001c0001t0004g0293 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1814+1149G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6606478 | ||||||
chr4:6606499
|
C | T | 1 | a0002c0002t0001g0171 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1814+1170C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6606499 | ||||||
chr4:6606502
|
C | T | 47 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(44): Show | 50 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.1814+1173C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6606502 | ||||||
chr4:6606708
|
T | C | 116 | a0001c0001t0001g0021a0001c0001t0001g0079a0001c0001t0001g0095others(113): Show | 117 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.1814+1379T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6606708 | ||||||
chr4:6606938
|
T | C | 6 | a0011c0009t0002g0048a0011c0009t0002g0222a0011c0009t0016g0026others(3): Show | 6 | HG02622.hp1 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1814+1609T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6606938 | ||||||
chr4:6607031
|
A | G | 4 | a0002c0002t0009g0025a0009c0011t0001g0046a0009c0011t0001g0105others(1): Show | 4 | HG02976.hp1 HG03130.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1814+1702A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6607031 | ||||||
chr4:6607041
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1814+1712C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6607041 | ||||||
chr4:6607079
|
G | A | 1 | a0040c0039t0007g0050 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1814+1750G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6607079 | ||||||
chr4:6607126
|
A | G | 1 | a0013c0053t0014g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1814+1797A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6607126 | ||||||
chr4:6607129
|
T | C | 202 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(199): Show | 211 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.1814+1800T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6607129 | ||||||
chr4:6607215
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1814+1886T>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6607215 | ||||||
chr4:6607449
|
C | T | 6 | a0011c0009t0002g0048a0011c0009t0002g0222a0011c0009t0016g0026others(3): Show | 6 | HG02622.hp1 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1815-1658C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6607449 | ||||||
chr4:6607494
|
C | G | 1 | a0001c0003t0003g0264 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1815-1613C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6607494 | ||||||
chr4:6607543
|
C | T | 1 | a0003c0044t0002g0132 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1815-1564C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6607543 | ||||||
chr4:6607599
|
G | T | 1 | a0002c0002t0001g0181 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1815-1508G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6607599 | ||||||
chr4:6607658
|
G | A | 13 | a0001c0054t0002g0220a0003c0007t0009g0041a0003c0007t0010g0007others(10): Show | 14 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.1815-1449G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6607658 | ||||||
chr4:6607813
|
T | C | 3 | a0002c0013t0001g0016a0002c0013t0022g0016a0029c0059t0001g0304 | 3 | NA18940.hp1 NA18977.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1815-1294T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6607813 | ||||||
chr4:6607822
|
C | T | 1 | a0002c0002t0001g0106 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1815-1285C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6607822 | ||||||
chr4:6608230
|
C | T | 44 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(41): Show | 47 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.1815-877C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6608230 | ||||||
chr4:6608294
|
T | A | 1 | a0011c0009t0032g0084 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1815-813T>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6608294 | ||||||
chr4:6608418
|
C | T | 107 | a0001c0001t0001g0021a0001c0001t0001g0079a0001c0001t0001g0095others(104): Show | 108 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1815-689C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6608418 | ||||||
chr4:6608592
|
T | G | 110 | a0001c0001t0001g0021a0001c0001t0001g0079a0001c0001t0001g0095others(107): Show | 111 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1815-515T>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6608592 | ||||||
chr4:6608629
|
C | T | 2 | a0002c0002t0001g0143a0044c0026t0001g0141 | 2 | HG01943.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1815-478C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6608629 | ||||||
chr4:6608772
|
T | C | 1 | a0042c0043t0030g0089 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1815-335T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6608772 | ||||||
chr4:6608895
|
C | T | 64 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(61): Show | 71 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.1815-212C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6608895 | ||||||
chr4:6608898
|
C | T | 9 | a0001c0055t0002g0122a0003c0041t0002g0076a0003c0070t0002g0034others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.1815-209C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6608898 | ||||||
chr4:6608941
|
C | T | 44 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(41): Show | 47 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.1815-166C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6608941 | ||||||
chr4:6609048
|
G | A | 12 | a0003c0007t0009g0041a0003c0007t0010g0007a0003c0007t0010g0042others(9): Show | 13 | HG00733.hp1 HG01884.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1815-59G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 11/18 | chr4 | 6609048 | ||||||
chr4:6609343
|
G | A | 2 | a0001c0001t0001g0259a0001c0001t0001g0261 | 2 | HG00621.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.2006+45G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 12/18 | chr4 | 6609343 | ||||||
chr4:6609511
|
TG | T | 72 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(69): Show | 79 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(76): Show |
intron_variant | MODIFIER | c.2006+216delG | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr4 | 6609511 | |||||
chr4:6609517
|
A | G | 1 | a0037c0047t0027g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2006+219A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 12/18 | chr4 | 6609517 | ||||||
chr4:6609665
|
T | C | 1 | a0007c0006t0001g0185 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2007-133T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 12/18 | chr4 | 6609665 | ||||||
chr4:6609691
|
G | A | 1 | a0002c0002t0001g0173 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2007-107G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 12/18 | chr4 | 6609691 | ||||||
chr4:6609746
|
G | A | 2 | a0001c0001t0001g0068a0001c0003t0002g0071 | 2 | NA18991.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2007-52G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 12/18 | chr4 | 6609746 | ||||||
chr4:6610086
|
T | C | 88 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(85): Show | 96 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.2259+36T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 13/18 | chr4 | 6610086 | ||||||
chr4:6610123
|
G | GCAGTAGA others(3): Show |
5 | a0011c0009t0002g0048a0011c0009t0002g0222a0011c0009t0016g0026others(2): Show | 5 | HG02723.hp2 HG02818.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2259+85_2259+94dup others(10): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr4 | 6610123 | |||||
chr4:6610366
|
A | C | 1 | a0002c0031t0005g0083 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2259+316A>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 13/18 | chr4 | 6610366 | ||||||
chr4:6610448
|
C | T | 1 | a0034c0056t0007g0221 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2259+398C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 13/18 | chr4 | 6610448 | ||||||
chr4:6610589
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2260-291G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 13/18 | chr4 | 6610589 | ||||||
chr4:6610595
|
C | T | 2 | a0002c0002t0001g0063a0002c0002t0001g0111 | 2 | HG02165.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.2260-285C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 13/18 | chr4 | 6610595 | ||||||
chr4:6610657
|
G | A | 84 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(81): Show | 90 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(87): Show |
intron_variant | MODIFIER | c.2260-223G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 13/18 | chr4 | 6610657 | ||||||
chr4:6610810
|
C | A | 6 | a0001c0054t0002g0220a0003c0044t0002g0132a0021c0020t0002g0045others(3): Show | 6 | HG00733.hp1 HG01884.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.2260-70C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 13/18 | chr4 | 6610810 | ||||||
chr4:6610828
|
C | A | 1 | a0002c0002t0001g0182 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2260-52C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 13/18 | chr4 | 6610828 | ||||||
chr4:6611005
|
C | G | 2 | a0021c0020t0002g0045a0042c0043t0030g0089 | 2 | HG01884.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2370+15C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 14/18 | chr4 | 6611005 | ||||||
chr4:6611296
|
C | A | 5 | a0013c0051t0001g0223a0013c0052t0003g0225a0013c0053t0014g0040others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2563+18C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6611296 | ||||||
chr4:6611333
|
C | G | 6 | a0001c0001t0001g0234a0011c0009t0002g0048a0011c0009t0002g0222others(3): Show | 6 | HG01175.hp2 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2563+55C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6611333 | ||||||
chr4:6611348
|
G | A | 7 | a0002c0013t0001g0016a0002c0013t0022g0016a0003c0007t0009g0041others(4): Show | 8 | HG02258.hp2 HG02559.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2563+70G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6611348 | ||||||
chr4:6611398
|
C | G | 1 | a0037c0047t0027g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2563+120C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6611398 | ||||||
chr4:6611469
|
G | C | 9 | a0003c0007t0009g0041a0003c0007t0010g0007a0003c0007t0010g0042others(6): Show | 10 | HG01109.hp1 HG01891.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.2563+191G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6611469 | ||||||
chr4:6611523
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2563+245C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6611523 | ||||||
chr4:6611525
|
T | G | 93 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(90): Show | 100 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(97): Show |
intron_variant | MODIFIER | c.2563+247T>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6611525 | ||||||
chr4:6611558
|
A | ATCTTTTC others(84): Show |
1 | a0013c0053t0014g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2563+294_2563+295i others(93): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 6611558 | |||||
chr4:6611558
|
A | ATCTTTTC others(88): Show |
1 | a0026c0066t0028g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2563+294_2563+295i others(97): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 6611558 | |||||
chr4:6611558
|
A | ATCTTTTC others(89): Show |
1 | a0013c0051t0001g0223 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2563+294_2563+295i others(98): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 6611558 | |||||
chr4:6611558
|
A | ATCTTTTC others(90): Show |
1 | a0003c0007t0010g0007 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.2563+294_2563+295i others(99): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 6611558 | |||||
chr4:6611558
|
A | ATCTTTTC others(91): Show |
1 | a0003c0007t0009g0041 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2563+294_2563+295i others(100): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 6611558 | |||||
chr4:6611558
|
A | ATCTTTTC others(92): Show |
2 | a0003c0007t0013g0057a0013c0052t0003g0225 | 2 | HG01891.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.2563+294_2563+295i others(101): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 6611558 | |||||
chr4:6611558
|
A | ATCTTTTC others(93): Show |
1 | a0003c0007t0010g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2563+294_2563+295i others(102): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 6611558 | |||||
chr4:6611641
|
C | T | 1 | a0002c0002t0001g0155 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2563+363C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6611641 | ||||||
chr4:6611719
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2563+441G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6611719 | ||||||
chr4:6611735
|
A | G | 68 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(65): Show | 74 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.2563+457A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6611735 | ||||||
chr4:6611759
|
A | G | 6 | a0001c0054t0002g0220a0003c0044t0002g0132a0021c0020t0002g0045others(3): Show | 6 | HG00733.hp1 HG01884.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.2563+481A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6611759 | ||||||
chr4:6611847
|
G | A | 4 | a0002c0002t0001g0006a0002c0002t0001g0318a0002c0002t0001g0319others(1): Show | 5 | HG00609.hp1 HG02015.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.2563+569G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6611847 | ||||||
chr4:6611878
|
A | G | 99 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(96): Show | 106 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.2563+600A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6611878 | ||||||
chr4:6611926
|
A | C | 13 | a0003c0007t0009g0041a0003c0007t0010g0007a0003c0007t0010g0042others(10): Show | 14 | HG01884.hp2 HG02257.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2563+648A>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6611926 | ||||||
chr4:6611989
|
T | C | 8 | a0003c0007t0009g0041a0003c0007t0010g0007a0003c0007t0010g0042others(5): Show | 9 | HG01109.hp1 HG01891.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.2563+711T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6611989 | ||||||
chr4:6612075
|
C | T | 1 | a0037c0047t0027g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2563+797C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6612075 | ||||||
chr4:6612185
|
C | T | 6 | a0001c0001t0001g0234a0011c0009t0002g0048a0011c0009t0002g0222others(3): Show | 6 | HG01175.hp2 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2563+907C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6612185 | ||||||
chr4:6612441
|
A | G | 98 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(95): Show | 105 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.2563+1163A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6612441 | ||||||
chr4:6612485
|
A | C | 1 | a0037c0047t0027g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2563+1207A>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6612485 | ||||||
chr4:6612656
|
GTCAGGT | G | 6 | a0003c0070t0002g0034a0006c0016t0006g0125a0016c0014t0006g0199others(3): Show | 6 | HG02572.hp2 HG02630.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.2563+1381_2563+138 others(10): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 6612656 | |||||
chr4:6612691
|
T | C | 1 | a0040c0039t0007g0050 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2563+1413T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6612691 | ||||||
chr4:6612732
|
A | G | 6 | a0001c0001t0001g0234a0011c0009t0002g0048a0011c0009t0002g0222others(3): Show | 6 | HG01175.hp2 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2563+1454A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6612732 | ||||||
chr4:6612798
|
G | A | 6 | a0001c0001t0001g0234a0011c0009t0002g0048a0011c0009t0002g0222others(3): Show | 6 | HG01175.hp2 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2564-1420G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6612798 | ||||||
chr4:6612916
|
G | A | 5 | a0001c0054t0002g0220a0003c0044t0002g0132a0021c0020t0002g0045others(2): Show | 5 | HG00733.hp1 HG01884.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.2564-1302G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6612916 | ||||||
chr4:6613029
|
G | C | 77 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(74): Show | 83 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(80): Show |
intron_variant | MODIFIER | c.2564-1189G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6613029 | ||||||
chr4:6613189
|
C | T | 6 | a0001c0001t0001g0234a0011c0009t0002g0048a0011c0009t0002g0222others(3): Show | 6 | HG01175.hp2 HG02723.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.2564-1029C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6613189 | ||||||
chr4:6613227
|
C | T | 62 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(59): Show | 68 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.2564-991C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6613227 | ||||||
chr4:6613248
|
T | C | 5 | a0011c0009t0002g0048a0011c0009t0002g0222a0011c0009t0016g0026others(2): Show | 5 | HG02723.hp2 HG02818.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.2564-970T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6613248 | ||||||
chr4:6613324
|
C | A | 2 | a0013c0051t0001g0223a0026c0066t0028g0131 | 2 | HG01109.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2564-894C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6613324 | ||||||
chr4:6613407
|
T | G | 9 | a0003c0041t0002g0076a0003c0070t0002g0034a0006c0016t0006g0125others(6): Show | 9 | HG01884.hp2 HG02257.hp1 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.2564-811T>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6613407 | ||||||
chr4:6613537
|
T | C | 1 | a0013c0051t0001g0223 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2564-681T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6613537 | ||||||
chr4:6613552
|
G | A | 1 | a0001c0001t0001g0263 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2564-666G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6613552 | ||||||
chr4:6613579
|
G | A | 1 | a0001c0003t0002g0186 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2564-639G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6613579 | ||||||
chr4:6613638
|
GGAAAAGA others(112): Show |
G | 1 | a0013c0053t0014g0040 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2564-563_2564-445d others(2): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 6613638 | |||||
chr4:6613655
|
TGGAAGGA others(112): Show |
T | 1 | a0039c0046t0017g0130 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2564-544_2564-426d others(2): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 6613655 | |||||
chr4:6613712
|
G | A | 5 | a0001c0001t0001g0234a0011c0009t0002g0048a0011c0009t0002g0222others(2): Show | 5 | HG01175.hp2 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2564-506G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6613712 | ||||||
chr4:6613760
|
AAAG | A | 28 | a0001c0001t0001g0165a0001c0001t0001g0269a0002c0002t0001g0006others(25): Show | 30 | HG00423.hp2 HG00558.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.2564-453_2564-451d others(5): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 6613760 | |||||
chr4:6613787
|
AGAAGGAA others(26): Show |
A | 7 | a0001c0054t0002g0220a0003c0044t0002g0132a0013c0051t0001g0223others(4): Show | 7 | HG00733.hp1 HG01109.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.2564-422_2564-390d others(35): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 6613787 | |||||
chr4:6613807
|
G | A | 1 | a0001c0001t0001g0086 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2564-411G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6613807 | ||||||
chr4:6613829
|
G | GA | 143 | a0001c0001t0001g0069a0001c0001t0001g0092a0001c0001t0001g0093others(140): Show | 154 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(151): Show |
intron_variant | MODIFIER | c.2564-383dupA | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr4 | 6613829 | |||||
chr4:6613890
|
G | A | 63 | a0001c0001t0001g0009a0001c0001t0001g0022a0001c0001t0001g0060others(60): Show | 69 | HG00140.hp2 HG00609.hp2 HG00639.hp2 others(66): Show |
intron_variant | MODIFIER | c.2564-328G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6613890 | ||||||
chr4:6613957
|
G | A | 2 | a0013c0053t0014g0040a0040c0039t0007g0050 | 2 | HG02280.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2564-261G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 15/18 | chr4 | 6613957 | ||||||
chr4:6614381
|
G | A | 1 | a0002c0004t0002g0188 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2701+26G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6614381 | ||||||
chr4:6614424
|
C | A | 3 | a0013c0053t0014g0040a0021c0020t0002g0045a0037c0047t0027g0195 | 3 | HG02622.hp1 HG02723.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2701+69C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6614424 | ||||||
chr4:6614482
|
T | C | 1 | a0037c0047t0027g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2701+127T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6614482 | ||||||
chr4:6614584
|
G | C | 1 | a0003c0007t0010g0042 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2701+229G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6614584 | ||||||
chr4:6614706
|
C | T | 5 | a0011c0009t0002g0048a0011c0009t0002g0222a0011c0009t0032g0084others(2): Show | 5 | HG02145.hp2 HG02723.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2701+351C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6614706 | ||||||
chr4:6614787
|
C | T | 60 | a0001c0001t0001g0128a0001c0001t0001g0134a0001c0001t0001g0234others(57): Show | 63 | HG00099.hp2 HG01175.hp2 HG01255.hp1 others(60): Show |
intron_variant | MODIFIER | c.2701+432C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6614787 | ||||||
chr4:6614805
|
G | A | 1 | a0002c0002t0002g0325 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2701+450G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6614805 | ||||||
chr4:6614848
|
G | A | 1 | a0002c0004t0011g0038 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2701+493G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6614848 | ||||||
chr4:6614933
|
G | T | 34 | a0001c0001t0001g0096a0001c0001t0001g0298a0001c0003t0002g0002others(31): Show | 37 | HG00140.hp1 HG00140.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.2701+578G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6614933 | ||||||
chr4:6614953
|
A | T | 156 | a0001c0001t0001g0065a0001c0001t0001g0086a0001c0001t0001g0096others(153): Show | 167 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.2701+598A>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6614953 | ||||||
chr4:6615012
|
T | C | 1 | a0002c0002t0001g0187 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.2701+657T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6615012 | ||||||
chr4:6615202
|
C | T | 4 | a0011c0009t0002g0048a0011c0009t0002g0222a0011c0009t0032g0084others(1): Show | 4 | HG02723.hp2 HG02818.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2701+847C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6615202 | ||||||
chr4:6615208
|
C | T | 217 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(214): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.2701+853C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6615208 | ||||||
chr4:6615221
|
T | C | 218 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(215): Show | 232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.2701+866T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6615221 | ||||||
chr4:6615439
|
G | C | 8 | a0002c0004t0031g0260a0002c0032t0011g0024a0003c0044t0002g0132others(5): Show | 8 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2701+1084G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6615439 | ||||||
chr4:6615478
|
A | T | 113 | a0001c0001t0001g0065a0001c0001t0001g0086a0001c0001t0001g0097others(110): Show | 121 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.2701+1123A>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6615478 | ||||||
chr4:6615480
|
C | T | 1 | a0002c0002t0001g0019 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.2701+1125C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6615480 | ||||||
chr4:6615484
|
C | A | 17 | a0001c0054t0002g0220a0002c0002t0002g0085a0002c0002t0002g0123others(14): Show | 17 | HG01243.hp1 HG02145.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.2701+1129C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6615484 | ||||||
chr4:6615498
|
A | G | 109 | a0001c0001t0001g0065a0001c0001t0001g0086a0001c0001t0001g0097others(106): Show | 117 | HG00408.hp1 HG00423.hp1 HG00558.hp1 others(114): Show |
intron_variant | MODIFIER | c.2701+1143A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6615498 | ||||||
chr4:6615595
|
G | A | 1 | a0001c0003t0003g0264 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2701+1240G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6615595 | ||||||
chr4:6615604
|
C | T | 4 | a0006c0016t0006g0125a0016c0014t0006g0199a0016c0014t0006g0200others(1): Show | 4 | HG02886.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2701+1249C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6615604 | ||||||
chr4:6615655
|
G | C | 10 | a0002c0004t0031g0260a0002c0032t0011g0024a0003c0044t0002g0132others(7): Show | 10 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.2701+1300G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6615655 | ||||||
chr4:6615768
|
C | T | 1 | a0002c0002t0001g0087 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2701+1413C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6615768 | ||||||
chr4:6615807
|
AT | A | 9 | a0002c0004t0031g0260a0002c0032t0011g0024a0003c0044t0002g0132others(6): Show | 9 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(6): Show |
intron_variant | MODIFIER | c.2701+1462delT | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | 6615807 | |||||
chr4:6615808
|
T | A | 1 | a0007c0006t0001g0156 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2701+1453T>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6615808 | ||||||
chr4:6615809
|
T | A | 8 | a0002c0004t0031g0260a0002c0032t0011g0024a0003c0044t0002g0132others(5): Show | 8 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2701+1454T>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6615809 | ||||||
chr4:6615899
|
G | T | 1 | a0037c0047t0027g0195 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2702-1481G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6615899 | ||||||
chr4:6615910
|
TCTC | T | 4 | a0002c0004t0031g0260a0003c0044t0002g0132a0010c0017t0002g0270others(1): Show | 4 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.2702-1467_2702-146 others(7): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | 6615910 | |||||
chr4:6616030
|
C | T | 150 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(147): Show | 162 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.2702-1350C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6616030 | ||||||
chr4:6616073
|
C | T | 1 | a0002c0002t0001g0289 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2702-1307C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6616073 | ||||||
chr4:6616219
|
T | C | 8 | a0002c0004t0031g0260a0002c0032t0011g0024a0003c0044t0002g0132others(5): Show | 8 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2702-1161T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6616219 | ||||||
chr4:6616275
|
C | A | 1 | a0024c0067t0025g0031 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2702-1105C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6616275 | ||||||
chr4:6616295
|
C | T | 2 | a0001c0001t0004g0281a0037c0047t0027g0195 | 2 | HG02622.hp1 NA18949.hp1 |
intron_variant | MODIFIER | c.2702-1085C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6616295 | ||||||
chr4:6616363
|
T | C | 8 | a0002c0004t0031g0260a0002c0032t0011g0024a0003c0044t0002g0132others(5): Show | 8 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2702-1017T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6616363 | ||||||
chr4:6616395
|
T | C | 12 | a0002c0004t0002g0188a0002c0004t0031g0260a0002c0032t0011g0024others(9): Show | 12 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.2702-985T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6616395 | ||||||
chr4:6616424
|
C | A | 4 | a0006c0016t0006g0125a0016c0014t0006g0199a0016c0014t0006g0200others(1): Show | 4 | HG02886.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2702-956C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6616424 | ||||||
chr4:6616437
|
C | T | 2 | a0002c0002t0001g0063a0002c0002t0001g0111 | 2 | HG02165.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.2702-943C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6616437 | ||||||
chr4:6616474
|
G | A | 8 | a0002c0004t0031g0260a0002c0032t0011g0024a0003c0044t0002g0132others(5): Show | 8 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2702-906G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6616474 | ||||||
chr4:6616539
|
G | A | 1 | a0043c0040t0015g0039 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2702-841G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6616539 | ||||||
chr4:6616598
|
A | C | 1 | a0001c0001t0001g0128 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2702-782A>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6616598 | ||||||
chr4:6616606
|
G | A | 2 | a0030c0058t0007g0127a0037c0047t0027g0195 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2702-774G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6616606 | ||||||
chr4:6616809
|
G | A | 3 | a0002c0032t0011g0024a0021c0020t0002g0045a0042c0043t0030g0089 | 3 | HG01884.hp1 HG03453.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2702-571G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6616809 | ||||||
chr4:6616810
|
C | T | 1 | a0001c0003t0002g0320 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2702-570C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6616810 | ||||||
chr4:6616834
|
C | T | 1 | a0006c0050t0026g0224 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2702-546C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6616834 | ||||||
chr4:6616835
|
G | A | 1 | a0002c0002t0001g0087 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2702-545G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6616835 | ||||||
chr4:6616847
|
C | T | 8 | a0002c0004t0031g0260a0002c0032t0011g0024a0003c0044t0002g0132others(5): Show | 8 | HG00733.hp1 HG01070.hp1 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2702-533C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6616847 | ||||||
chr4:6616869
|
C | T | 1 | a0002c0033t0001g0145 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2702-511C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6616869 | ||||||
chr4:6616951
|
G | A | 1 | a0026c0066t0028g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2702-429G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6616951 | ||||||
chr4:6617048
|
G | A | 24 | a0001c0054t0002g0220a0002c0002t0002g0085a0002c0002t0002g0123others(21): Show | 24 | HG01243.hp1 HG02145.hp1 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.2702-332G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6617048 | ||||||
chr4:6617075
|
G | A | 4 | a0006c0016t0006g0125a0016c0014t0006g0199a0016c0014t0006g0200others(1): Show | 4 | HG02886.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2702-305G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6617075 | ||||||
chr4:6617153
|
G | GAC | 3 | a0002c0004t0003g0203a0002c0004t0003g0323a0009c0028t0003g0047 | 3 | HG02809.hp1 HG02976.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.2702-226_2702-225d others(4): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr4 | 6617153 | |||||
chr4:6617277
|
A | G | 284 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(281): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.2702-103A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6617277 | ||||||
chr4:6617325
|
A | G | 279 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(276): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.2702-55A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6617325 | ||||||
chr4:6617651
|
T | C | 39 | a0001c0003t0002g0002a0001c0003t0002g0027a0001c0003t0002g0054others(36): Show | 41 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(38): Show |
intron_variant | MODIFIER | c.2814+159T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6617651 | ||||||
chr4:6617760
|
A | ATTTTTTT others(82): Show |
1 | a0001c0001t0001g0313 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.2814+268_2814+269i others(91): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6617760 | ||||||
chr4:6617838
|
G | A | 3 | a0002c0032t0011g0024a0021c0020t0002g0045a0042c0043t0030g0089 | 3 | HG01884.hp1 HG03453.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2814+346G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6617838 | ||||||
chr4:6617839
|
A | C | 44 | a0001c0003t0002g0002a0001c0003t0002g0027a0001c0003t0002g0054others(41): Show | 46 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(43): Show |
intron_variant | MODIFIER | c.2814+347A>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6617839 | ||||||
chr4:6617846
|
AG | A | 37 | a0001c0003t0002g0002a0001c0003t0002g0027a0001c0003t0002g0054others(34): Show | 39 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(36): Show |
intron_variant | MODIFIER | c.2814+355delG | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6617846 | ||||||
chr4:6617847
|
G | GT | 23 | a0001c0001t0001g0068a0001c0054t0002g0220a0002c0002t0001g0144others(20): Show | 23 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.2814+372dupT | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr4 | 6617847 | |||||
chr4:6617847
|
G | GTT | 223 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(220): Show | 241 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.2814+371_2814+372d others(4): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr4 | 6617847 | |||||
chr4:6617847
|
G | GTTT | 14 | a0001c0001t0001g0101a0001c0001t0001g0253a0001c0001t0001g0259others(11): Show | 14 | HG00621.hp2 HG00642.hp1 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.2814+370_2814+372d others(5): Show |
MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr4 | 6617847 | |||||
chr4:6617865
|
G | C | 1 | a0006c0016t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2814+373G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6617865 | ||||||
chr4:6617870
|
C | G | 39 | a0001c0003t0002g0002a0001c0003t0002g0027a0001c0003t0002g0054others(36): Show | 41 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(38): Show |
intron_variant | MODIFIER | c.2814+378C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6617870 | ||||||
chr4:6617878
|
G | A | 1 | a0002c0002t0001g0152 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.2814+386G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6617878 | ||||||
chr4:6617884
|
G | A | 1 | a0021c0020t0002g0049 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2814+392G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6617884 | ||||||
chr4:6617886
|
C | T | 1 | a0006c0050t0026g0224 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2814+394C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6617886 | ||||||
chr4:6617887
|
C | G | 29 | a0001c0003t0003g0228a0001c0003t0003g0264a0002c0004t0002g0188others(26): Show | 31 | HG01255.hp1 HG01891.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.2814+395C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6617887 | ||||||
chr4:6617910
|
C | T | 47 | a0001c0003t0003g0228a0001c0003t0003g0264a0001c0054t0002g0220others(44): Show | 49 | HG01109.hp1 HG01243.hp1 HG01255.hp1 others(46): Show |
intron_variant | MODIFIER | c.2814+418C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6617910 | ||||||
chr4:6617926
|
C | T | 1 | a0002c0002t0001g0169 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2814+434C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6617926 | ||||||
chr4:6617955
|
C | A | 1 | a0001c0001t0001g0311 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2814+463C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6617955 | ||||||
chr4:6617972
|
C | G | 3 | a0002c0002t0009g0025a0009c0011t0001g0046a0009c0011t0001g0105 | 3 | HG02976.hp1 HG03130.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.2814+480C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6617972 | ||||||
chr4:6617972
|
C | T | 1 | a0002c0002t0001g0183 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2814+480C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6617972 | ||||||
chr4:6617977
|
A | G | 1 | a0002c0002t0001g0051 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.2814+485A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6617977 | ||||||
chr4:6618009
|
G | A | 1 | a0008c0008t0005g0011 | 2 | HG01167.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.2814+517G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6618009 | ||||||
chr4:6618069
|
C | T | 1 | a0030c0058t0007g0127 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2814+577C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6618069 | ||||||
chr4:6618130
|
G | A | 1 | a0001c0001t0001g0103 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2814+638G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6618130 | ||||||
chr4:6618152
|
G | A | 2 | a0002c0002t0001g0063a0002c0002t0001g0111 | 2 | HG02165.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.2814+660G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6618152 | ||||||
chr4:6618170
|
G | A | 1 | a0009c0011t0001g0046 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2814+678G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6618170 | ||||||
chr4:6618206
|
G | A | 3 | a0002c0032t0011g0024a0021c0020t0002g0045a0042c0043t0030g0089 | 3 | HG01884.hp1 HG03453.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2814+714G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6618206 | ||||||
chr4:6618209
|
C | T | 1 | a0001c0001t0004g0293 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2814+717C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6618209 | ||||||
chr4:6618291
|
A | G | 19 | a0001c0054t0002g0220a0002c0002t0002g0085a0002c0002t0002g0123others(16): Show | 19 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.2814+799A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6618291 | ||||||
chr4:6618356
|
T | G | 28 | a0001c0003t0003g0228a0001c0003t0003g0264a0002c0004t0002g0188others(25): Show | 30 | HG01255.hp1 HG01891.hp1 HG02056.hp1 others(27): Show |
intron_variant | MODIFIER | c.2814+864T>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6618356 | ||||||
chr4:6618389
|
G | C | 15 | a0001c0054t0002g0220a0002c0002t0002g0085a0002c0002t0002g0123others(12): Show | 15 | HG01243.hp1 HG01884.hp2 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.2814+897G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6618389 | ||||||
chr4:6618614
|
C | T | 1 | a0021c0020t0002g0049 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2814+1122C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6618614 | ||||||
chr4:6618813
|
C | T | 2 | a0006c0016t0003g0271a0012c0049t0003g0098 | 2 | HG03704.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.2815-1114C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6618813 | ||||||
chr4:6618871
|
G | A | 4 | a0006c0016t0006g0125a0016c0014t0006g0199a0016c0014t0006g0200others(1): Show | 4 | HG02886.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2815-1056G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6618871 | ||||||
chr4:6618875
|
C | G | 229 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(226): Show | 247 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.2815-1052C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6618875 | ||||||
chr4:6618876
|
G | A | 1 | a0026c0066t0028g0131 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2815-1051G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6618876 | ||||||
chr4:6618983
|
A | G | 289 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(286): Show | 309 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(306): Show |
intron_variant | MODIFIER | c.2815-944A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6618983 | ||||||
chr4:6618985
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.2815-942C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6618985 | ||||||
chr4:6619082
|
C | A | 2 | a0001c0001t0001g0235a0002c0002t0001g0242 | 2 | HG02129.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.2815-845C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6619082 | ||||||
chr4:6619254
|
G | C | 1 | a0014c0012t0002g0197 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2815-673G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6619254 | ||||||
chr4:6619264
|
A | G | 331 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(328): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.2815-663A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6619264 | ||||||
chr4:6619370
|
A | G | 335 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(332): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.2815-557A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6619370 | ||||||
chr4:6619377
|
A | G | 326 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(323): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2815-550A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6619377 | ||||||
chr4:6619461
|
G | C | 295 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(292): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.2815-466G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6619461 | ||||||
chr4:6619502
|
C | T | 2 | a0006c0050t0026g0224a0037c0047t0027g0195 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2815-425C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6619502 | ||||||
chr4:6619527
|
G | A | 5 | a0030c0058t0007g0127a0034c0056t0007g0221a0040c0039t0007g0050others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.2815-400G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6619527 | ||||||
chr4:6619532
|
G | A | 1 | a0002c0004t0008g0191 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2815-395G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6619532 | ||||||
chr4:6619574
|
G | T | 1 | a0032c0071t0003g0333 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2815-353G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6619574 | ||||||
chr4:6619597
|
G | T | 11 | a0001c0054t0002g0220a0002c0002t0002g0085a0002c0002t0002g0123others(8): Show | 11 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.2815-330G>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6619597 | ||||||
chr4:6619632
|
G | A | 1 | a0038c0045t0002g0082 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2815-295G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6619632 | ||||||
chr4:6620073
|
C | T | 3 | a0003c0036t0002g0036a0022c0037t0003g0124a0022c0069t0003g0033 | 3 | HG03041.hp1 HG03579.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2932+29C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6620073 | ||||||
chr4:6620115
|
G | A | 2 | a0001c0001t0001g0308a0001c0001t0001g0321 | 2 | NA18999.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.2932+71G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6620115 | ||||||
chr4:6620140
|
G | A | 1 | a0006c0016t0002g0126 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2932+96G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6620140 | ||||||
chr4:6620201
|
T | C | 335 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(332): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.2932+157T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6620201 | ||||||
chr4:6620302
|
T | A | 12 | a0002c0004t0003g0078a0002c0004t0003g0196a0002c0004t0003g0203others(9): Show | 13 | HG01255.hp1 HG02109.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.2932+258T>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6620302 | ||||||
chr4:6620408
|
G | A | 4 | a0006c0016t0006g0125a0016c0014t0006g0199a0016c0014t0006g0200others(1): Show | 4 | HG02886.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2932+364G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6620408 | ||||||
chr4:6620413
|
C | A | 42 | a0001c0003t0002g0002a0001c0003t0002g0027a0001c0003t0002g0054others(39): Show | 44 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.2932+369C>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6620413 | ||||||
chr4:6620444
|
C | G | 331 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(328): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.2932+400C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6620444 | ||||||
chr4:6620454
|
G | A | 15 | a0001c0054t0002g0220a0002c0002t0002g0085a0002c0002t0002g0123others(12): Show | 15 | HG01109.hp1 HG01243.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.2932+410G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6620454 | ||||||
chr4:6620459
|
A | G | 1 | a0002c0002t0001g0332 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2932+415A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6620459 | ||||||
chr4:6620517
|
C | T | 4 | a0006c0016t0006g0125a0016c0014t0006g0199a0016c0014t0006g0200others(1): Show | 4 | HG02886.hp1 HG03130.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2932+473C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6620517 | ||||||
chr4:6620581
|
G | C | 326 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(323): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2932+537G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6620581 | ||||||
chr4:6620631
|
G | A | 1 | a0002c0002t0001g0146 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.2933-557G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6620631 | ||||||
chr4:6620701
|
T | G | 2 | a0006c0050t0026g0224a0037c0047t0027g0195 | 2 | HG02451.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2933-487T>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6620701 | ||||||
chr4:6620738
|
T | C | 1 | a0002c0002t0001g0153 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2933-450T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6620738 | ||||||
chr4:6620744
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2933-444A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6620744 | ||||||
chr4:6620817
|
G | A | 1 | a0001c0001t0001g0231 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.2933-371G>A | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6620817 | ||||||
chr4:6620920
|
A | G | 326 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0022others(323): Show | 348 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(345): Show |
intron_variant | MODIFIER | c.2933-268A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6620920 | ||||||
chr4:6620967
|
G | C | 1 | a0001c0001t0001g0263 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.2933-221G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6620967 | ||||||
chr4:6621059
|
T | C | 31 | a0001c0003t0003g0228a0001c0003t0003g0264a0002c0002t0001g0106others(28): Show | 33 | HG01175.hp1 HG01255.hp1 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.2933-129T>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6621059 | ||||||
chr4:6621178
|
G | C | 12 | a0002c0004t0003g0078a0002c0004t0003g0196a0002c0004t0003g0203others(9): Show | 13 | HG01255.hp1 HG02109.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.2933-10G>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6621178 |