Item | Value |
---|---|
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 | 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 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0002 | 0/1 | 1009 | 126 | 25 | 25 | 56 | 5 | 14 | 37 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0003 | 0/0 | 1009 | 12 | 11 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0004 | 0/0 | 1009 | 9 | 1 | 7 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0005 | 1/0 | 1009 | 5 | 3 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0006 | 0/0 | 1009 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0007 | 0/0 | 1009 | 5 | 1 | 1 | 2 | 1 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0008 | 0/0 | 1009 | 5 | 3 | 0 | 1 | 0 | 1 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0009 | 0/0 | 1009 | 4 | 0 | 4 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0010 | 0/0 | 1009 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0011 | 0/0 | 1009 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0012 | 0/0 | 1009 | 3 | 0 | 0 | 0 | 1 | 2 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0013 | 0/0 | 1009 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0014 | 0/0 | 1009 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0015 | 0/0 | 1009 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0016 | 0/0 | 1009 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0017 | 0/0 | 1009 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0018 | 0/0 | 1009 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0019 | 0/0 | 1009 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0020 | 0/0 | 1009 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0021 | 0/0 | 1009 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0022 | 0/0 | 1009 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0023 | 0/0 | 1009 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0024 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0025 | 0/0 | 1009 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0026 | 0/0 | 1009 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0027 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0028 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0029 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0030 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0031 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0032 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0033 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0034 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0035 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0036 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0037 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0038 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0039 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0040 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0041 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0042 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0043 | 0/0 | 1009 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
a0044 | 0/0 | 1009 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | MGQLC others(1004): Show |
chr4 | 6570189 | 6628362 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3027 | 107 | 2 | 22 | 72 | 2 | 9 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0001c0003 | 0/0 | 3027 | 22 | 1 | 0 | 15 | 1 | 5 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0001c0054 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0001c0055 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0001c0061 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0001c0064 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0002c0002 | 0/1 | 3027 | 98 | 11 | 22 | 49 | 3 | 12 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0002c0004 | 0/0 | 3027 | 21 | 11 | 2 | 4 | 2 | 2 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0002c0013 | 0/0 | 3027 | 3 | 0 | 1 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0002c0030 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0002c0031 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0002c0032 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0002c0033 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0003c0007 | 0/0 | 3027 | 5 | 5 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0003c0015 | 0/0 | 3027 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0003c0036 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0003c0041 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0003c0044 | 0/0 | 3027 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0003c0070 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0004c0005 | 0/0 | 3027 | 9 | 1 | 7 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0005c0008 | 1/0 | 3027 | 4 | 2 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0005c0038 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0006c0010 | 0/0 | 3027 | 4 | 4 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0006c0021 | 0/0 | 3027 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0007c0006 | 0/0 | 3027 | 5 | 1 | 1 | 2 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0008c0016 | 0/0 | 3027 | 3 | 2 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0008c0050 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0008c0057 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0009c0017 | 0/0 | 3027 | 3 | 0 | 3 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0009c0060 | 0/0 | 3027 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0010c0009 | 0/0 | 3027 | 4 | 4 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0011c0011 | 0/0 | 3027 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0011c0028 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0012c0022 | 0/0 | 3027 | 2 | 0 | 0 | 0 | 1 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0012c0049 | 0/0 | 3027 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0013c0019 | 0/0 | 3027 | 2 | 1 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0013c0035 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0014c0051 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0014c0052 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0014c0053 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0015c0012 | 0/0 | 3027 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0016c0014 | 0/0 | 3027 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0017c0024 | 0/0 | 3027 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0018c0023 | 0/0 | 3027 | 2 | 0 | 1 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0019c0020 | 0/0 | 3027 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0020c0037 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0020c0069 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0021c0018 | 0/0 | 3027 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0022c0025 | 0/0 | 3027 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0023c0066 | 0/0 | 3027 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0024c0043 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0025c0065 | 0/0 | 3027 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0026c0026 | 0/0 | 3027 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0027c0063 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0028c0045 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0029c0042 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0030c0067 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0031c0039 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0032c0047 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0033c0058 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0034c0046 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0035c0056 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0036c0068 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0037c0040 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0038c0048 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0039c0062 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0040c0027 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0041c0059 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0042c0034 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0043c0071 | 0/0 | 3027 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 | ||
a0044c0029 | 0/0 | 3027 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ATGGG others(3022): Show |
chr4 | 6570189 | 6628362 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5130 | 98 | 2 | 18 | 68 | 2 | 8 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0001c0001t0003 | 0/0 | 5131 | 5 | 0 | 1 | 4 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5126): Show |
chr4 | 6570189 | 6628362 |
a0001c0001t0011 | 0/0 | 5130 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0001c0001t0017 | 0/0 | 5130 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0001c0001t0018 | 0/0 | 5130 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0001c0001t0022 | 0/0 | 5129 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0001c0003t0002 | 0/0 | 5129 | 22 | 1 | 0 | 15 | 1 | 5 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0001c0054t0002 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0001c0055t0002 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0001c0061t0001 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0001c0064t0001 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0002c0002t0001 | 0/0 | 5130 | 86 | 5 | 21 | 46 | 3 | 11 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0002c0002t0002 | 0/0 | 5129 | 5 | 4 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0002c0002t0003 | 0/0 | 5131 | 2 | 0 | 0 | 1 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5126): Show |
chr4 | 6570189 | 6628362 |
a0002c0002t0008 | 0/0 | 5130 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0002c0002t0019 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0002c0002t0023 | 0/1 | 5129 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0002c0002t0029 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0002c0004t0002 | 0/0 | 5129 | 17 | 10 | 1 | 4 | 1 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0002c0004t0007 | 0/0 | 5129 | 2 | 0 | 1 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0002c0004t0010 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0002c0004t0027 | 0/0 | 5129 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0002c0013t0001 | 0/0 | 5130 | 2 | 0 | 1 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0002c0013t0021 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0002c0030t0012 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0002c0031t0004 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0002c0032t0010 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0002c0033t0001 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0003c0007t0008 | 0/0 | 5130 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0003c0007t0009 | 0/0 | 5129 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0003c0007t0012 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0003c0015t0002 | 0/0 | 5129 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0003c0036t0002 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0003c0041t0002 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0003c0044t0002 | 0/0 | 5129 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0003c0070t0002 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0004c0005t0001 | 0/0 | 5130 | 9 | 1 | 7 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0005c0008t0004 | 1/0 | 5129 | 4 | 2 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0005c0038t0011 | 0/0 | 5130 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0006c0010t0002 | 0/0 | 5129 | 4 | 4 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0006c0021t0001 | 0/0 | 5130 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0007c0006t0001 | 0/0 | 5130 | 5 | 1 | 1 | 2 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0008c0016t0002 | 0/0 | 5129 | 2 | 1 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0008c0016t0005 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0008c0050t0024 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0008c0057t0001 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0009c0017t0002 | 0/0 | 5129 | 3 | 0 | 3 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0009c0060t0001 | 0/0 | 5130 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0010c0009t0002 | 0/0 | 5129 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0010c0009t0015 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0010c0009t0028 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0011c0011t0001 | 0/0 | 5130 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0011c0011t0002 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0011c0028t0002 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0012c0022t0001 | 0/0 | 5130 | 2 | 0 | 0 | 0 | 1 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0012c0049t0002 | 0/0 | 5129 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0013c0019t0001 | 0/0 | 5130 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0013c0019t0002 | 0/0 | 5129 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0013c0035t0002 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0014c0051t0001 | 0/0 | 5130 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0014c0052t0002 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0014c0053t0013 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0015c0012t0002 | 0/0 | 5129 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0016c0014t0005 | 0/0 | 5129 | 3 | 3 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0017c0024t0007 | 0/0 | 5129 | 2 | 0 | 2 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0018c0023t0001 | 0/0 | 5130 | 2 | 0 | 1 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0019c0020t0002 | 0/0 | 5129 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0020c0037t0002 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0020c0069t0002 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0021c0018t0001 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0021c0018t0020 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0022c0025t0001 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0022c0025t0003 | 0/0 | 5131 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5126): Show |
chr4 | 6570189 | 6628362 |
a0023c0066t0002 | 0/0 | 5129 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0024c0043t0026 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0025c0065t0003 | 0/0 | 5131 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5126): Show |
chr4 | 6570189 | 6628362 |
a0026c0026t0001 | 0/0 | 5130 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0027c0063t0001 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0028c0045t0002 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0029c0042t0006 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(4521): Show |
chr4 | 6570189 | 6628362 |
a0030c0067t0001 | 0/0 | 5130 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0031c0039t0006 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(4521): Show |
chr4 | 6570189 | 6628362 |
a0032c0047t0025 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0033c0058t0006 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(4521): Show |
chr4 | 6570189 | 6628362 |
a0034c0046t0016 | 0/0 | 5460 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5455): Show |
chr4 | 6570189 | 6628362 |
a0035c0056t0006 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(4521): Show |
chr4 | 6570189 | 6628362 |
a0036c0068t0001 | 0/0 | 5130 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0037c0040t0014 | 0/0 | 4526 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(4521): Show |
chr4 | 6570189 | 6628362 |
a0038c0048t0001 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0039c0062t0001 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0040c0027t0001 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0041c0059t0001 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0042c0034t0001 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
a0043c0071t0002 | 0/0 | 5129 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5124): Show |
chr4 | 6570189 | 6628362 |
a0044c0029t0001 | 0/0 | 5130 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | ACCTT others(5125): Show |
chr4 | 6570189 | 6628362 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0091 | 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 |
a0001c0001t0001g0094 | 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 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0246 | 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 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0001c0001t0001g0265 | 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 |
a0001c0001t0001g0274 | 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 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0279 | 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 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0289 | 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 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0304 | 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 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 1 | 0 | 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 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0011g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0017g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0018g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0001t0022g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0003t0002g0313 | 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 |
a0001c0055t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0061t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0001c0064t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0001 | 0/0 | 7 | 0 | 2 | 5 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0004 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0005 | 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 |
a0002c0002t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0023 | 0/0 | 2 | 0 | 2 | 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 |
a0002c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0103 | 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 |
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 |
a0002c0002t0001g0115 | 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 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | 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 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0270 | 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 |
a0002c0002t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0003g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0003g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0008g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0019g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0023g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0002t0029g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0002g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0002c0004t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 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 |
a0002c0004t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0002g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0007g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0007g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0010g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0004t0027g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0013t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0013t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0013t0021g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0030t0012g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0031t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0032t0010g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0002c0033t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0003c0007t0008g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0003c0007t0009g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0003c0007t0009g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0003c0007t0012g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0003c0015t0002g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0003c0015t0002g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0003c0036t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0003c0041t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0003c0044t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0003c0070t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0004c0005t0001g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0004c0005t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0004c0005t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0004c0005t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0004c0005t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0004c0005t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0005c0008t0004g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0005c0008t0004g0013 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0005c0038t0011g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0006c0010t0002g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0006c0010t0002g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0006c0021t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0007c0006t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0007c0006t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0007c0006t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0007c0006t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0007c0006t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0008c0016t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0008c0016t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0008c0016t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0008c0050t0024g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0008c0057t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0009c0017t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0009c0017t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0009c0017t0002g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0009c0060t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0010c0009t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0010c0009t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0010c0009t0015g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0010c0009t0028g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0011c0011t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0011c0011t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0011c0011t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0011c0028t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0012c0022t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0012c0022t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0012c0049t0002g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0013c0019t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0013c0019t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0013c0035t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0014c0051t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0014c0052t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0014c0053t0013g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0015c0012t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0015c0012t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0015c0012t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0016c0014t0005g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0016c0014t0005g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0016c0014t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0017c0024t0007g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0017c0024t0007g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0018c0023t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0018c0023t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0019c0020t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0019c0020t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0020c0037t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0020c0069t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0021c0018t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0021c0018t0020g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0022c0025t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0022c0025t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0023c0066t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0024c0043t0026g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0025c0065t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0026c0026t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0027c0063t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0028c0045t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0029c0042t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0030c0067t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0031c0039t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0032c0047t0025g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0033c0058t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0034c0046t0016g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0035c0056t0006g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0036c0068t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0037c0040t0014g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0038c0048t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0039c0062t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0040c0027t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0041c0059t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0042c0034t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0043c0071t0002g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
a0044c0029t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 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 | g0124 | EUR | GBR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00099 | hp2 | a0002 | c0004 | t0007 | g0179 | EUR | GBR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00140 | hp1 | a0002 | c0004 | t0002 | g0201 | EUR | GBR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00140 | hp2 | a0001 | c0003 | t0002 | g0168 | EUR | GBR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00323 | hp1 | a0002 | c0002 | t0001 | g0174 | EUR | FIN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00323 | hp2 | a0012 | c0022 | t0001 | g0263 | EUR | FIN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0116 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0247 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0241 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0182 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0299 | 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 | g0014 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0139 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00639 | hp2 | a0017 | c0024 | t0007 | g0098 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00642 | hp2 | a0009 | c0017 | t0002 | g0261 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00733 | hp1 | a0003 | c0044 | t0002 | g0213 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0034 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00738 | hp1 | a0004 | c0005 | t0001 | g0195 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG00738 | hp2 | a0017 | c0024 | t0007 | g0064 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01069 | hp1 | a0002 | c0013 | t0001 | g0180 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0023 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01070 | hp1 | a0009 | c0017 | t0002 | g0306 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0311 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0023 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01071 | hp2 | a0009 | c0017 | t0002 | g0268 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0264 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0169 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01106 | hp1 | a0018 | c0023 | t0001 | g0262 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01109 | hp1 | a0023 | c0066 | t0002 | g0205 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0029 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01167 | hp2 | a0005 | c0008 | t0004 | g0012 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01168 | hp2 | a0004 | c0005 | t0001 | g0160 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01169 | hp2 | a0004 | c0005 | t0001 | g0159 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01175 | hp1 | a0002 | c0002 | t0002 | g0227 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01243 | hp1 | a0013 | c0019 | t0002 | g0129 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01255 | hp1 | a0002 | c0004 | t0002 | g0194 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0035 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01256 | hp1 | a0001 | c0001 | t0022 | g0198 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0171 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01261 | hp1 | a0002 | c0002 | t0001 | g0204 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0203 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0202 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01358 | hp2 | a0001 | c0001 | t0018 | g0056 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01361 | hp1 | a0001 | c0001 | t0017 | g0024 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01361 | hp2 | a0007 | c0006 | t0001 | g0075 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | CLM | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0166 | EUR | IBS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | IBS | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01884 | hp1 | a0024 | c0043 | t0026 | g0071 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01884 | hp2 | a0003 | c0041 | t0002 | g0082 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01891 | hp1 | a0014 | c0052 | t0002 | g0248 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01891 | hp2 | a0006 | c0021 | t0001 | g0008 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01928 | hp1 | a0004 | c0005 | t0001 | g0199 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01928 | hp2 | a0025 | c0065 | t0003 | g0131 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0154 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0196 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01943 | hp2 | a0026 | c0026 | t0001 | g0127 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0140 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01952 | hp2 | a0004 | c0005 | t0001 | g0002 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0271 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01978 | hp2 | a0002 | c0004 | t0007 | g0178 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG01993 | hp2 | a0009 | c0060 | t0001 | g0236 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02004 | hp2 | a0004 | c0005 | t0001 | g0002 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0287 | 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 | g0001 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02055 | hp1 | a0007 | c0006 | t0001 | g0063 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0249 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02056 | hp1 | a0001 | c0003 | t0002 | g0267 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02056 | hp2 | a0001 | c0003 | t0002 | g0251 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0117 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02071 | hp2 | a0007 | c0006 | t0001 | g0144 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0017 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0137 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02129 | hp1 | a0027 | c0063 | t0001 | g0233 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0260 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0314 | 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 | g0002 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0312 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02145 | hp1 | a0002 | c0002 | t0002 | g0039 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02145 | hp2 | a0028 | c0045 | t0002 | g0065 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02148 | hp1 | a0004 | c0005 | t0001 | g0002 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0133 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0290 | 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 | g0085 | EAS | CDX | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | CDX | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02257 | hp1 | a0019 | c0020 | t0002 | g0054 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02257 | hp2 | a0029 | c0042 | t0006 | g0060 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02258 | hp1 | a0030 | c0067 | t0001 | g0037 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02258 | hp2 | a0003 | c0007 | t0009 | g0048 | 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 | g0309 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02280 | hp1 | a0006 | c0010 | t0002 | g0011 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02280 | hp2 | a0031 | c0039 | t0006 | g0049 | 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 | g0100 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0244 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0102 | AMR | PEL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02451 | hp1 | a0008 | c0050 | t0024 | g0222 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02451 | hp2 | a0013 | c0035 | t0002 | g0151 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0108 | EAS | KHV | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02572 | hp1 | a0001 | c0003 | t0002 | g0187 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02572 | hp2 | a0003 | c0070 | t0002 | g0042 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02602 | hp2 | a0001 | c0003 | t0002 | g0275 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02615 | hp1 | a0006 | c0010 | t0002 | g0009 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02615 | hp2 | a0002 | c0031 | t0004 | g0066 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02622 | hp1 | a0032 | c0047 | t0025 | g0183 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02622 | hp2 | a0002 | c0004 | t0002 | g0192 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02630 | hp1 | a0003 | c0007 | t0012 | g0070 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02630 | hp2 | a0033 | c0058 | t0006 | g0210 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02647 | hp1 | a0002 | c0004 | t0002 | g0193 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02647 | hp2 | a0034 | c0046 | t0016 | g0123 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02683 | hp2 | a0002 | c0002 | t0001 | g0021 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02717 | hp1 | a0005 | c0008 | t0004 | g0013 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02717 | hp2 | a0003 | c0015 | t0002 | g0025 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02723 | hp1 | a0014 | c0053 | t0013 | g0046 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02723 | hp2 | a0010 | c0009 | t0002 | g0051 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02809 | hp1 | a0002 | c0004 | t0002 | g0317 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02809 | hp2 | a0002 | c0004 | t0002 | g0175 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02818 | hp1 | a0002 | c0002 | t0002 | g0068 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02818 | hp2 | a0010 | c0009 | t0028 | g0067 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02886 | hp1 | a0008 | c0016 | t0005 | g0208 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02886 | hp2 | a0006 | c0010 | t0002 | g0009 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02895 | hp1 | a0003 | c0015 | t0002 | g0025 | 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 | t0009 | g0007 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02896 | hp2 | a0002 | c0004 | t0002 | g0191 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02897 | hp1 | a0003 | c0007 | t0009 | g0007 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02897 | hp2 | a0003 | c0015 | t0002 | g0320 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02965 | hp1 | a0006 | c0010 | t0002 | g0011 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02965 | hp2 | a0001 | c0055 | t0002 | g0214 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02970 | hp1 | a0015 | c0012 | t0002 | g0189 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0005 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02976 | hp1 | a0002 | c0002 | t0008 | g0031 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02976 | hp2 | a0002 | c0004 | t0002 | g0188 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03017 | hp1 | a0012 | c0022 | t0001 | g0286 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0163 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03041 | hp1 | a0003 | c0036 | t0002 | g0040 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03041 | hp2 | a0035 | c0056 | t0006 | g0219 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03130 | hp1 | a0011 | c0011 | t0001 | g0107 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03130 | hp2 | a0016 | c0014 | t0005 | g0186 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03139 | hp1 | a0016 | c0014 | t0005 | g0184 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03139 | hp2 | a0011 | c0011 | t0002 | g0106 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03195 | hp1 | a0002 | c0002 | t0002 | g0319 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03195 | hp2 | a0008 | c0016 | t0002 | g0209 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03209 | hp1 | a0011 | c0028 | t0002 | g0053 | AFR | MSL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03209 | hp2 | a0036 | c0068 | t0001 | g0038 | AFR | MSL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03239 | hp1 | a0002 | c0004 | t0002 | g0146 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0177 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03453 | hp1 | a0019 | c0020 | t0002 | g0050 | AFR | MSL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03453 | hp2 | a0011 | c0011 | t0001 | g0052 | AFR | MSL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03486 | hp1 | a0037 | c0040 | t0014 | g0045 | AFR | MSL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03486 | hp2 | a0002 | c0004 | t0002 | g0061 | 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 | g0005 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0128 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03492 | hp2 | a0002 | c0002 | t0001 | g0005 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03516 | hp1 | a0010 | c0009 | t0002 | g0221 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0172 | AFR | ESN | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03540 | hp1 | a0015 | c0012 | t0002 | g0197 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03540 | hp2 | a0005 | c0008 | t0004 | g0012 | AFR | GWD | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03579 | hp1 | a0020 | c0037 | t0002 | g0207 | AFR | MSL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03579 | hp2 | a0002 | c0030 | t0012 | g0215 | AFR | MSL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0084 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03669 | hp1 | a0018 | c0023 | t0001 | g0167 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03669 | hp2 | a0001 | c0003 | t0002 | g0058 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03688 | hp1 | a0002 | c0002 | t0003 | g0121 | SAS | STU | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0149 | SAS | STU | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03704 | hp2 | a0012 | c0049 | t0002 | g0101 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03710 | hp2 | a0001 | c0003 | t0002 | g0147 | SAS | PJL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03831 | hp1 | a0001 | c0001 | t0011 | g0036 | SAS | BEB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03831 | hp2 | a0008 | c0016 | t0002 | g0297 | SAS | BEB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0004 | SAS | BEB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | BEB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG04184 | hp2 | a0001 | c0003 | t0002 | g0033 | SAS | BEB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG04204 | hp1 | a0001 | c0003 | t0002 | g0092 | SAS | STU | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG04204 | hp2 | a0002 | c0002 | t0001 | g0165 | SAS | STU | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18522 | hp1 | a0002 | c0004 | t0002 | g0010 | AFR | YRI | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18522 | hp2 | a0002 | c0004 | t0010 | g0044 | AFR | YRI | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18612 | hp1 | a0001 | c0003 | t0002 | g0083 | EAS | CHB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0055 | EAS | CHB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | CHB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | CHB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18906 | hp1 | a0010 | c0009 | t0015 | g0032 | AFR | YRI | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18906 | hp2 | a0002 | c0002 | t0002 | g0206 | AFR | YRI | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18940 | hp1 | a0002 | c0013 | t0021 | g0019 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18941 | hp2 | a0038 | c0048 | t0001 | g0111 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18942 | hp1 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18944 | hp2 | a0021 | c0018 | t0001 | g0026 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18948 | hp1 | a0002 | c0002 | t0019 | g0020 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18949 | hp1 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18949 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18950 | hp2 | a0001 | c0003 | t0002 | g0292 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18952 | hp1 | a0001 | c0003 | t0002 | g0285 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0323 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0134 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18953 | hp2 | a0039 | c0062 | t0001 | g0104 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18954 | hp1 | a0002 | c0002 | t0001 | g0270 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0074 | 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 | g0265 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18957 | hp2 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0158 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18962 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18963 | hp1 | a0022 | c0025 | t0001 | g0176 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18963 | hp2 | a0002 | c0004 | t0002 | g0216 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0308 | 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 | g0226 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18965 | hp2 | a0022 | c0025 | t0003 | g0153 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18966 | hp1 | a0002 | c0002 | t0029 | g0143 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18966 | hp2 | a0001 | c0064 | t0001 | g0225 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18967 | hp2 | a0002 | c0033 | t0001 | g0135 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18970 | hp2 | a0001 | c0003 | t0002 | g0250 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18971 | hp1 | a0021 | c0018 | t0020 | g0026 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18971 | hp2 | a0002 | c0004 | t0002 | g0156 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0240 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18977 | hp1 | a0041 | c0059 | t0001 | g0252 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18980 | hp1 | a0001 | c0061 | t0001 | g0089 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0181 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18982 | hp2 | a0001 | c0003 | t0002 | g0088 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18983 | hp2 | a0001 | c0003 | t0002 | g0077 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18990 | hp2 | a0007 | c0006 | t0001 | g0141 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18991 | hp2 | a0001 | c0003 | t0002 | g0096 | 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 | g0003 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18997 | hp2 | a0001 | c0003 | t0002 | g0097 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0136 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0277 | 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 | g0269 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19007 | hp2 | a0001 | c0003 | t0002 | g0313 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19011 | hp1 | a0002 | c0002 | t0001 | g0288 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19012 | hp1 | a0042 | c0034 | t0001 | g0142 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19030 | hp1 | a0013 | c0019 | t0001 | g0072 | AFR | LWK | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19030 | hp2 | a0006 | c0021 | t0001 | g0008 | AFR | LWK | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19043 | hp1 | a0043 | c0071 | t0002 | g0325 | AFR | LWK | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19043 | hp2 | a0016 | c0014 | t0005 | g0185 | AFR | LWK | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0103 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19060 | hp2 | a0001 | c0003 | t0002 | g0003 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19063 | hp1 | a0001 | c0003 | t0002 | g0059 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19063 | hp2 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19065 | hp2 | a0002 | c0002 | t0001 | g0115 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0162 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19074 | hp1 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19074 | hp2 | a0044 | c0029 | t0001 | g0212 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19080 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19081 | hp1 | a0008 | c0057 | t0001 | g0303 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19081 | hp2 | a0002 | c0002 | t0001 | g0157 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19082 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19085 | hp1 | a0002 | c0004 | t0002 | g0217 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19090 | hp2 | a0002 | c0002 | t0001 | g0155 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19091 | hp1 | a0002 | c0013 | t0001 | g0019 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA20129 | hp1 | a0020 | c0069 | t0002 | g0041 | AFR | ASW | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | ASW | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0161 | EUR | TSI | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA20752 | hp2 | a0007 | c0006 | t0001 | g0173 | EUR | TSI | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0228 | SAS | GIH | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA20905 | hp2 | a0002 | c0004 | t0027 | g0266 | SAS | GIH | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02109 | hp2 | a0015 | c0012 | t0002 | g0190 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0069 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02486 | hp2 | a0002 | c0004 | t0002 | g0010 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02559 | hp1 | a0002 | c0004 | t0002 | g0200 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG02559 | hp2 | a0003 | c0007 | t0008 | g0047 | AFR | ACB | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0148 | AFR | MSL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG03471 | hp2 | a0014 | c0051 | t0001 | g0218 | AFR | MSL | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG06807 | hp1 | a0004 | c0005 | t0001 | g0021 | AFR | USA | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
HG06807 | hp2 | a0002 | c0002 | t0008 | g0043 | AFR | USA | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA18955 | hp2 | a0040 | c0027 | t0001 | g0110 | EAS | JPT | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA20300 | hp1 | a0005 | c0038 | t0011 | g0057 | AFR | USA | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
NA20300 | hp2 | a0002 | c0032 | t0010 | g0030 | AFR | USA | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
homoSapiens | chm13v2 | a0002 | c0002 | t0023 | g0164 | REF | REF | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
homoSapiens | grch38p0 | a0005 | c0008 | t0004 | g0013 | REF | REF | MAN2B2_chr4_6570189_6628362 | MAN2B2 | chr4 | 6570189 | 6628362 |
view | 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 | a0026 | 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 | a0040 | 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 | a0011 | 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 | a0023 a0030 a0036 |
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 | a0001 a0008 a0009 others(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 | a0025 | 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 | a0002 a0004 a0007 others(11): Show |
160 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(157): 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 | a0032 | 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 | a0006 a0028 a0034 |
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 | a0001 a0003 a0006 others(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 | a0022 | 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 | a0001 a0003 a0006 others(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 | a0044 | 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 | a0017 | 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 | a0009 | 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 | a0042 | 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 | a0010 a0015 a0032 |
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 | a0010 a0015 a0032 |
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 | a0014 a0023 a0024 |
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 | a0041 | 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 | a0021 | 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 | a0035 | 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 | a0013 | 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 | a0034 | 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 | a0027 | 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 | a0004 a0020 a0043 |
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 | a0029 a0031 a0033 others(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 | a0039 | 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 | a0029 a0031 a0033 others(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 |
view | 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 | a0003c0070 a0020c0069 a0043c0071 |
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 | a0003c0036 a0006c0010 a0006c0021 others(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 | a0001c0054 a0001c0055 a0003c0015 others(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 | a0031c0039 | 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 | a0002c0013 a0041c0059 |
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 | a0002c0030 a0030c0067 |
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 | a0003c0041 a0014c0053 |
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 | a0001c0001 a0001c0003 a0001c0054 others(65): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): 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 | a0001c0001 a0001c0054 a0001c0061 others(28): Show |
257 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(254): 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 | a0023c0066 | 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 |
view | 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 | a0002c0002t0029 | 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 | a0002c0002t0008 a0002c0004t0010 a0002c0032t0010 others(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 | 83 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0011 others(80): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): 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 | a0002c0030t0012 a0003c0007t0009 a0003c0007t0012 |
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 | a0029c0042t0006 a0031c0039t0006 a0033c0058t0006 others(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 | a0010c0009t0015 a0010c0009t0028 |
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 | a0008c0016t0005 a0016c0014t0005 |
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 | 42 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0017 others(39): Show |
247 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(244): 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 | a0002c0004t0007 a0017c0024t0007 |
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 | a0008c0050t0024 | 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 | a0001c0001t0017 | 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 | a0001c0001t0018 | 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 | a0002c0002t0019 | 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 | a0032c0047t0025 | 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 | a0002c0004t0027 | 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 | a0021c0018t0020 | 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 | a0029c0042t0006 a0031c0039t0006 a0033c0058t0006 others(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 | a0002c0013t0021 | 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 | 39 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0017 others(36): Show |
239 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(236): 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 | a0001c0001t0003 a0002c0002t0003 a0022c0025t0003 others(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 | a0024c0043t0026 | 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 | a0034c0046t0016 | 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 | a0002c0002t0001 | 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 | a0008c0016t0005 a0016c0014t0005 |
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 | 87 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0011 others(84): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): 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 | a0030c0067t0001 | 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 | a0001c0003t0002 a0002c0002t0002 a0002c0004t0002 others(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 | a0034c0046t0016 | 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 | a0002c0004t0027 | 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 | 82 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0011 others(79): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): 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 | a0008c0016t0005 a0008c0050t0024 a0016c0014t0005 others(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 | 81 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0011 others(78): Show |
342 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(339): Show |
3_prime_UTR_variant | MODIFIER | c.*2067A>C | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 19/19 | 2067 | chr4 | 6623352 |
view | 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 | a0001c0001t0001g0027 | 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 | a0043c0071t0002g0325 | 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 | a0001c0001t0001g0028 | 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 | a0001c0001t0001g0028 | 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 | a0001c0001t0001g0028 | 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 | a0002c0002t0001g0029 | 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 | a0001c0001t0001g0028 | 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 | a0002c0002t0008g0031 a0002c0032t0010g0030 a0010c0009t0015g0032 |
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 | a0001c0003t0002g0033 | 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 | a0001c0001t0001g0324 a0002c0002t0001g0323 a0021c0018t0001g0026 others(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 | a0001c0001t0001g0322 | 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 | a0002c0002t0001g0034 a0002c0002t0001g0035 |
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 | a0001c0001t0011g0036 | 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 | a0030c0067t0001g0037 a0036c0068t0001g0038 |
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 | a0001c0001t0001g0321 | 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 | a0002c0002t0002g0039 a0002c0002t0008g0031 a0002c0002t0008g0043 others(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 | a0003c0007t0008g0047 a0003c0007t0009g0007 a0003c0007t0009g0048 |
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 | 8 | a0006c0010t0002g0009 a0006c0021t0001g0008 a0010c0009t0002g0051 others(5): 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 | 4 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0010c0009t0015g0032 others(1): 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 | a0002c0002t0001g0034 | 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 | a0002c0002t0001g0055 | 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 | 273 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0027 others(270): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.285+36A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 2/18 | chr4 | 6576760 | |||||||
chr4:6576887 | C | T | 5 | a0002c0002t0002g0319 a0003c0015t0002g0025 a0003c0015t0002g0320 others(2): 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 | a0001c0001t0001g0318 | 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 | a0001c0001t0001g0028 | 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 | a0002c0002t0001g0029 | 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 | a0002c0004t0002g0317 | 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 | 10 | a0006c0010t0002g0009 a0006c0021t0001g0008 a0010c0009t0002g0051 others(7): 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 | a0002c0002t0008g0043 a0002c0004t0010g0044 a0014c0053t0013g0046 others(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 | 5 | a0002c0002t0002g0319 a0003c0015t0002g0025 a0003c0015t0002g0320 others(2): 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 | a0003c0007t0008g0047 a0003c0007t0009g0007 a0003c0007t0009g0048 |
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 | 103 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0223 others(100): 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 | 5 | a0002c0002t0002g0319 a0003c0015t0002g0025 a0003c0015t0002g0320 others(2): 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 | a0001c0054t0002g0220 a0008c0050t0024g0222 a0010c0009t0002g0221 others(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 | a0001c0001t0001g0028 | 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 | a0014c0053t0013g0046 a0037c0040t0014g0045 |
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 | a0001c0001t0018g0056 | 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 | a0005c0038t0011g0057 | 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 | a0001c0003t0002g0058 | 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 | a0002c0002t0008g0043 a0014c0053t0013g0046 a0037c0040t0014g0045 |
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 | 4 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0010c0009t0015g0032 others(1): 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 | 112 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(109): 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 | 4 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0010c0009t0015g0032 others(1): 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 | a0039c0062t0001g0104 | 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 | 18 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(15): 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 | a0001c0001t0001g0316 | 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 | a0001c0001t0001g0315 | 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 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 |
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 | a0001c0001t0001g0062 a0001c0001t0001g0122 a0001c0003t0002g0059 others(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 | 1 | a0002c0004t0002g0010 | 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 | a0001c0054t0002g0220 a0010c0009t0002g0221 a0035c0056t0006g0219 |
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 | a0001c0055t0002g0214 a0002c0002t0008g0043 a0030c0067t0001g0037 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0093 a0001c0001t0001g0094 others(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 | 67 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0074 others(64): 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 | a0002c0002t0003g0121 | 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 | a0002c0002t0001g0117 | 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 | a0001c0001t0001g0119 | 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 | a0002c0002t0001g0116 | 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 | a0001c0001t0001g0118 a0002c0002t0001g0015 a0002c0002t0001g0055 others(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 | a0002c0002t0001g0016 a0002c0002t0001g0114 |
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 | a0001c0001t0001g0120 | 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 | a0002c0002t0001g0017 | 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 | a0002c0002t0001g0017 | 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 | a0038c0048t0001g0111 | 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 | a0009c0017t0002g0261 | 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 | a0002c0004t0002g0216 a0002c0004t0002g0217 |
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 | a0002c0002t0001g0240 | 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 | a0001c0003t0002g0285 | 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 | a0040c0027t0001g0110 | 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 | a0001c0003t0002g0033 | 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 | a0001c0003t0002g0033 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0074 others(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 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
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 | a0023c0066t0002g0205 | 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 | a0003c0044t0002g0213 | 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 | a0002c0002t0001g0323 a0021c0018t0001g0026 a0021c0018t0020g0026 |
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 | a0004c0005t0001g0159 a0004c0005t0001g0160 |
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 | 4 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0010c0009t0015g0032 others(1): 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 | a0003c0044t0002g0213 | 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 | a0023c0066t0002g0205 | 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 | a0001c0003t0002g0251 | 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 | a0001c0001t0001g0102 | 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 | 3 | a0001c0003t0002g0251 a0002c0002t0001g0103 a0006c0010t0002g0009 |
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 | a0001c0001t0001g0022 a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0001g0022 | 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 | a0002c0002t0001g0103 | 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 | 1 | a0006c0010t0002g0009 | 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 | 1 | a0006c0010t0002g0009 | 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 | 25 | a0001c0001t0001g0022 a0001c0001t0001g0118 a0001c0001t0001g0119 others(22): 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 | a0010c0009t0015g0032 | 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 |
3 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0043c0071t0002g0325 |
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 | a0012c0022t0001g0286 | 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 | a0002c0013t0001g0180 | 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 | a0003c0007t0012g0070 | 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 | a0002c0002t0001g0103 a0002c0030t0012g0215 |
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 | 5 | a0001c0001t0001g0022 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): 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 | a0001c0064t0001g0225 | 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 | a0001c0001t0001g0237 | 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 | a0001c0001t0001g0226 | 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 | a0002c0002t0002g0227 | 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 | a0001c0001t0001g0234 | 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 | a0001c0001t0001g0228 | 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 | a0001c0001t0001g0229 | 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 | a0001c0001t0001g0230 | 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 | a0027c0063t0001g0233 | 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 | a0002c0002t0001g0023 | 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 | a0001c0001t0003g0232 | 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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0235 | 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 | a0009c0060t0001g0236 | 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 | a0001c0001t0001g0238 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0242 a0001c0001t0003g0243 others(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 | a0002c0002t0001g0240 | 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 | a0002c0002t0001g0244 | 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 | a0001c0001t0001g0245 | 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 | a0001c0001t0001g0246 | 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 | a0002c0002t0001g0034 | 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 | a0002c0002t0001g0247 | 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 | a0001c0055t0002g0214 a0002c0002t0008g0043 |
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 | a0001c0001t0001g0239 | 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 | a0002c0002t0001g0241 | 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 | a0001c0001t0001g0310 | 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 | a0001c0001t0001g0302 a0001c0001t0001g0309 |
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 | a0001c0001t0001g0289 a0001c0001t0001g0290 a0001c0001t0001g0293 others(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 | a0001c0001t0001g0291 | 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 | 51 | a0001c0001t0001g0105 a0001c0001t0001g0239 a0001c0001t0001g0254 others(48): 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 | a0001c0001t0001g0316 | 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 | a0002c0002t0001g0249 | 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 | a0041c0059t0001g0252 | 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 | a0002c0002t0001g0034 | 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 | 165 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(162): 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 | a0013c0019t0002g0129 | 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 | a0002c0030t0012g0215 | 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 | a0001c0001t0001g0256 | 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 | a0001c0001t0001g0259 | 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 | a0009c0017t0002g0261 | 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 | a0018c0023t0001g0262 | 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 | a0012c0022t0001g0263 | 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 | a0002c0002t0001g0264 | 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 | a0002c0004t0027g0266 | 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 | a0001c0001t0001g0105 | 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 | a0009c0017t0002g0268 | 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 | a0001c0001t0003g0271 | 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 | a0001c0003t0002g0275 | 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 | a0001c0001t0001g0277 | 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 | a0001c0001t0001g0076 | 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 | a0005c0038t0011g0057 | 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 | a0001c0003t0002g0077 | 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 | a0001c0001t0001g0078 | 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 | a0002c0002t0001g0006 a0002c0002t0001g0287 a0002c0002t0001g0288 others(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 | a0044c0029t0001g0212 | 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 | a0003c0044t0002g0213 | 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 | 38 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0223 others(35): 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 | a0011c0011t0001g0052 a0011c0011t0001g0107 a0011c0011t0002g0106 others(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 | a0001c0003t0002g0033 | 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 | a0001c0001t0001g0102 a0002c0002t0001g0247 |
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 | a0001c0001t0001g0272 | 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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0274 | 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 | a0001c0003t0002g0251 | 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 | a0001c0001t0001g0254 | 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 | a0001c0001t0001g0269 | 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 | a0002c0002t0001g0270 | 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 | a0007c0006t0001g0075 | 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 | a0003c0070t0002g0042 a0020c0069t0002g0041 |
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 | 19 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(16): 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 | a0001c0003t0002g0250 | 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 | a0001c0001t0001g0276 | 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 | a0001c0001t0001g0265 | 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 | a0001c0003t0002g0267 | 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 | a0001c0001t0001g0282 a0001c0001t0001g0283 |
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 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 others(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 | a0001c0001t0001g0284 | 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 | a0001c0003t0002g0285 | 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 | a0023c0066t0002g0205 | 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 | a0001c0001t0001g0102 a0001c0001t0001g0229 a0001c0001t0001g0230 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0102 a0002c0002t0001g0103 |
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 | a0001c0001t0001g0254 a0001c0001t0001g0276 a0002c0002t0001g0023 others(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 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 others(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 | a0012c0022t0001g0286 | 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 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0003g0281 others(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 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0079 others(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 | a0001c0054t0002g0220 a0008c0050t0024g0222 a0010c0009t0002g0051 others(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 | a0002c0002t0001g0202 a0002c0002t0001g0203 a0002c0002t0001g0204 others(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 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0003g0281 others(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 | a0024c0043t0026g0071 | 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 | 91 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0079 others(88): 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 | a0001c0001t0001g0253 a0001c0003t0002g0058 |
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 | a0001c0001t0001g0246 | 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 | a0001c0001t0001g0253 a0001c0003t0002g0058 |
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 | a0001c0001t0001g0226 a0001c0001t0001g0235 a0001c0001t0001g0237 others(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 | a0014c0052t0002g0248 | 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 |
15 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(12): 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 | a0002c0002t0003g0121 | 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 | a0001c0001t0001g0255 | 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 | 23 | a0001c0001t0022g0198 a0001c0003t0002g0187 a0002c0002t0001g0021 others(20): 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 | a0003c0070t0002g0042 a0020c0069t0002g0041 |
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 | a0032c0047t0025g0183 | 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 | 3 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0043c0071t0002g0325 |
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 | a0010c0009t0015g0032 | 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 | a0001c0001t0001g0316 a0001c0003t0002g0058 a0002c0002t0001g0023 |
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 | a0001c0001t0003g0281 | 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 | 53 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0223 others(50): 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 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0280 others(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 | a0001c0001t0001g0226 a0001c0001t0001g0237 a0001c0003t0002g0077 others(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 | a0002c0002t0001g0108 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0245 | 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 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
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 | 70 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0076 others(67): 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 | a0001c0001t0001g0226 a0001c0001t0001g0237 a0001c0001t0001g0254 others(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 | a0002c0002t0001g0260 | 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 | 64 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0076 others(61): 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 | 3 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0043c0071t0002g0325 |
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 | a0001c0001t0001g0076 a0001c0001t0001g0269 a0002c0002t0001g0109 others(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 | 107 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0076 others(104): 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 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0079 others(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 | a0002c0002t0001g0128 | 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 | a0002c0002t0001g0103 | 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 | a0001c0001t0001g0235 a0001c0001t0001g0265 a0001c0001t0001g0278 others(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 | a0039c0062t0001g0104 | 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 | a0001c0001t0001g0078 a0001c0001t0001g0226 a0001c0001t0001g0237 others(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 | a0001c0001t0001g0253 a0012c0022t0001g0286 |
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 | a0001c0001t0001g0078 a0001c0001t0001g0226 a0001c0001t0001g0235 others(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 | a0001c0001t0001g0296 | 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 | a0010c0009t0015g0032 | 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 | a0001c0001t0001g0028 a0001c0001t0001g0079 a0001c0001t0001g0278 others(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 | 113 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(110): 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 | 3 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0043c0071t0002g0325 |
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 | a0001c0001t0001g0276 a0003c0007t0008g0047 a0003c0007t0009g0007 others(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 | a0011c0011t0001g0052 a0011c0011t0001g0107 a0011c0011t0002g0106 others(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 | a0001c0001t0001g0105 | 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 | 22 | a0001c0001t0001g0022 a0001c0001t0001g0223 a0001c0001t0001g0224 others(19): 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 | a0001c0001t0001g0254 a0001c0001t0001g0322 a0009c0060t0001g0236 |
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 | a0024c0043t0026g0071 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0242 a0001c0001t0001g0265 others(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 | a0024c0043t0026g0071 | 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 | a0001c0001t0001g0291 | 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 | a0002c0002t0001g0202 a0002c0002t0001g0203 a0002c0004t0002g0201 |
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 | a0002c0002t0001g0204 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0086 a0001c0001t0001g0087 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0079 a0001c0001t0001g0226 others(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 | a0001c0001t0001g0295 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0024 a0001c0001t0001g0086 others(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 | a0019c0020t0002g0054 | 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 | a0019c0020t0002g0050 a0031c0039t0006g0049 |
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 | a0001c0001t0001g0076 a0001c0001t0001g0229 a0001c0001t0001g0230 others(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 | a0001c0001t0001g0078 a0009c0060t0001g0236 a0030c0067t0001g0037 others(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 | a0001c0001t0001g0239 | 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 | a0019c0020t0002g0054 | 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 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0105 others(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 | a0001c0001t0001g0239 a0019c0020t0002g0054 |
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 | a0001c0001t0001g0226 a0001c0001t0001g0237 a0001c0001t0001g0238 others(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 | a0001c0001t0001g0246 a0001c0001t0001g0272 a0001c0001t0001g0273 others(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 | a0001c0001t0001g0228 | 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 | a0001c0001t0001g0234 | 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 | a0002c0002t0002g0227 | 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 |
3 | a0001c0001t0001g0022 a0001c0001t0001g0223 a0001c0001t0001g0224 |
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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0314 | 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 | a0019c0020t0002g0050 a0031c0039t0006g0049 |
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 | a0001c0001t0001g0294 | 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 | a0008c0016t0002g0297 | 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 | a0001c0001t0001g0300 | 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 | a0001c0001t0001g0304 a0001c0001t0003g0305 a0008c0057t0001g0303 |
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 | a0002c0002t0001g0035 | 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 | a0001c0001t0001g0307 | 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 | a0002c0002t0001g0312 | 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 | a0001c0001t0001g0301 | 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 | a0001c0001t0001g0310 | 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 | a0001c0003t0002g0313 | 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 | a0001c0001t0001g0308 | 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 | a0001c0001t0001g0302 a0001c0001t0001g0309 a0001c0001t0001g0311 others(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 | a0001c0001t0001g0293 | 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 | a0001c0001t0001g0254 a0002c0002t0001g0103 a0011c0011t0001g0052 others(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 | a0001c0001t0001g0028 a0001c0001t0001g0079 a0001c0001t0018g0056 |
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 | a0001c0001t0001g0014 a0001c0001t0001g0086 a0001c0001t0001g0087 others(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 | 84 | a0001c0001t0001g0022 a0001c0001t0001g0076 a0001c0001t0001g0078 others(81): 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 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0242 others(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 |
1 | a0006c0010t0002g0009 | 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 | a0001c0001t0001g0254 a0002c0002t0001g0249 |
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 | a0001c0001t0001g0024 a0001c0001t0017g0024 a0002c0002t0001g0103 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0076 a0001c0001t0001g0231 others(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 | a0044c0029t0001g0212 | 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 | a0001c0001t0001g0231 | 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 | a0001c0001t0001g0255 | 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 | a0002c0002t0001g0006 a0002c0002t0001g0287 a0002c0002t0003g0006 |
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 | a0002c0002t0001g0288 | 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 | a0001c0001t0011g0036 | 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 |
21 | a0001c0001t0001g0130 a0001c0001t0001g0132 a0001c0001t0001g0145 others(18): 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 | a0001c0001t0001g0256 a0001c0001t0001g0259 a0001c0001t0001g0277 others(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 | a0001c0001t0001g0074 | 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 | a0002c0004t0002g0317 a0003c0041t0002g0082 a0008c0016t0002g0297 |
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 | a0007c0006t0001g0075 | 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 | a0001c0001t0001g0300 | 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 | a0010c0009t0002g0051 | 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 | a0006c0021t0001g0008 | 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 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0002c0002t0001g0182 |
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 | a0030c0067t0001g0037 a0036c0068t0001g0038 |
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 | 69 | a0001c0001t0001g0022 a0001c0001t0001g0119 a0001c0001t0001g0120 others(66): 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 | a0001c0001t0001g0229 | 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 | a0001c0001t0001g0024 a0001c0001t0017g0024 |
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 | a0001c0001t0001g0105 | 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 | a0001c0001t0001g0298 | 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 | a0013c0019t0002g0129 | 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 | 29 | a0001c0001t0001g0022 a0001c0001t0001g0080 a0001c0001t0001g0081 others(26): 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 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0235 others(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 | a0001c0001t0001g0238 a0001c0001t0001g0254 a0001c0001t0001g0301 |
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 | a0001c0001t0001g0074 a0001c0001t0001g0080 a0001c0001t0001g0081 others(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 | a0001c0001t0001g0301 | 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 | 54 | a0001c0001t0001g0022 a0001c0001t0001g0080 a0001c0001t0001g0081 others(51): 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 | a0001c0001t0001g0024 a0001c0001t0001g0105 a0001c0001t0001g0229 others(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 | a0001c0001t0001g0078 | 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 | a0001c0001t0001g0226 | 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 | a0002c0002t0001g0260 | 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 | a0001c0001t0001g0253 | 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 | a0001c0001t0001g0237 | 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 | a0001c0001t0001g0296 | 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 | a0001c0003t0002g0267 | 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 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
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 | a0001c0001t0001g0321 | 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 | a0002c0030t0012g0215 | 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 | a0002c0004t0002g0200 a0003c0036t0002g0040 a0015c0012t0002g0197 |
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 | a0002c0004t0002g0194 | 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 | a0001c0001t0001g0235 a0001c0001t0003g0232 a0002c0002t0001g0244 |
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 | a0001c0001t0001g0315 | 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 | a0001c0001t0001g0276 | 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 | a0001c0001t0001g0245 a0001c0001t0001g0289 a0001c0001t0001g0290 others(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 | 29 | a0001c0001t0001g0022 a0001c0001t0001g0223 a0001c0001t0001g0224 others(26): 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 | 67 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0074 others(64): 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 | a0001c0001t0001g0245 a0001c0001t0001g0278 a0001c0001t0001g0279 others(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 | a0002c0002t0001g0241 | 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 | a0002c0002t0008g0031 | 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 | a0001c0001t0001g0314 | 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 | 48 | a0001c0001t0001g0024 a0001c0001t0001g0105 a0001c0001t0001g0118 others(45): 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 | a0001c0003t0002g0251 | 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 | 33 | a0001c0001t0001g0022 a0001c0001t0001g0223 a0001c0001t0001g0224 others(30): 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 | a0001c0001t0001g0074 a0001c0001t0001g0102 a0001c0003t0002g0059 others(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 | a0001c0003t0002g0077 | 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 | a0039c0062t0001g0104 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0078 others(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 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0001c0001t0001g0278 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0276 a0001c0001t0001g0315 |
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 | 78 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0073 others(75): 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 | a0001c0001t0001g0119 a0001c0001t0001g0120 a0003c0070t0002g0042 others(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 |
14 | a0001c0001t0001g0118 a0002c0002t0001g0015 a0002c0002t0001g0016 others(11): 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 | 13 | a0001c0054t0002g0220 a0006c0010t0002g0009 a0008c0050t0024g0222 others(10): 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 | a0001c0001t0001g0235 a0001c0001t0003g0232 a0002c0002t0001g0177 others(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 | a0002c0002t0001g0148 | 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 | a0006c0021t0001g0008 a0010c0009t0002g0051 |
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 | a0009c0060t0001g0236 | 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 | a0001c0001t0001g0272 | 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 | a0001c0001t0001g0294 | 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 | a0001c0001t0001g0289 | 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 | a0012c0022t0001g0286 | 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 | a0002c0002t0001g0247 | 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 | a0001c0001t0001g0290 | 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 | a0001c0001t0001g0278 a0001c0001t0001g0279 a0001c0001t0001g0282 others(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 | a0001c0001t0001g0280 a0001c0001t0001g0284 |
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 | a0002c0002t0001g0034 | 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 | a0001c0001t0003g0281 | 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 | a0001c0001t0001g0242 a0001c0001t0003g0243 |
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 | a0002c0002t0001g0240 | 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 | a0001c0001t0001g0230 | 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 | a0002c0002t0001g0249 | 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 | a0001c0001t0001g0291 | 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 | a0002c0004t0002g0217 | 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 | a0002c0002t0001g0181 | 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 | a0001c0064t0001g0225 | 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 | a0001c0001t0001g0295 | 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 | a0001c0003t0002g0292 | 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 | a0001c0001t0001g0245 | 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 | a0002c0002t0001g0299 | 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 | a0001c0001t0001g0238 | 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 | a0001c0003t0002g0285 | 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 | a0001c0001t0001g0269 | 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 | 72 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(69): 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 | a0010c0009t0015g0032 | 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 | a0002c0002t0008g0031 | 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 | a0001c0055t0002g0214 a0002c0002t0008g0043 a0014c0053t0013g0046 others(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 | a0002c0030t0012g0215 a0030c0067t0001g0037 a0036c0068t0001g0038 |
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 | a0001c0001t0001g0276 a0001c0003t0002g0147 |
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 | a0001c0055t0002g0214 a0002c0002t0008g0043 a0003c0007t0008g0047 others(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 | a0030c0067t0001g0037 a0036c0068t0001g0038 |
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 | a0001c0003t0002g0147 | 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 | a0005c0038t0011g0057 | 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 | 166 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(163): 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 | 126 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(123): 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 | a0002c0002t0001g0182 | 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 | a0002c0002t0001g0182 | 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 | a0002c0002t0001g0182 | 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 | 1 | a0002c0004t0002g0010 | 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 | a0002c0002t0001g0182 | 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 | a0002c0002t0001g0182 | 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 | a0001c0001t0001g0290 | 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 | a0003c0007t0008g0047 a0003c0007t0009g0007 a0003c0007t0009g0048 |
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 | 122 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(119): 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 | a0003c0070t0002g0042 a0020c0069t0002g0041 |
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 | a0003c0070t0002g0042 a0020c0069t0002g0041 |
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 | a0003c0070t0002g0042 a0020c0069t0002g0041 |
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 | a0003c0070t0002g0042 a0020c0069t0002g0041 |
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 | a0003c0070t0002g0042 | 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 | a0001c0001t0001g0316 | 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 | 122 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(119): 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 | a0002c0002t0001g0015 a0002c0002t0001g0016 a0002c0002t0001g0113 others(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 | a0001c0003t0002g0187 a0002c0004t0002g0188 a0002c0004t0002g0191 others(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 | a0001c0055t0002g0214 a0002c0002t0008g0043 a0003c0007t0008g0047 others(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 | 127 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(124): 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 | a0001c0055t0002g0214 a0002c0002t0008g0043 a0014c0053t0013g0046 others(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 | 122 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(119): 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 | a0005c0038t0011g0057 | 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 | 104 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(101): 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 | 18 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(15): 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 | a0030c0067t0001g0037 a0036c0068t0001g0038 |
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 | 141 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(138): 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 | 122 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(119): 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 | 122 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(119): 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 | 10 | a0006c0010t0002g0009 a0006c0021t0001g0008 a0010c0009t0002g0051 others(7): 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 | a0002c0002t0002g0068 | 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 | a0001c0001t0001g0027 | 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 | 153 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(150): 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 | 122 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(119): 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 | a0003c0007t0008g0047 a0003c0007t0009g0007 a0003c0007t0009g0048 |
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 | a0002c0004t0002g0175 a0034c0046t0016g0123 |
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 | 142 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(139): 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 | a0030c0067t0001g0037 a0036c0068t0001g0038 |
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 | 122 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(119): 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 | a0001c0055t0002g0214 a0002c0002t0008g0043 a0014c0053t0013g0046 others(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 | 20 | a0001c0054t0002g0220 a0002c0004t0002g0061 a0003c0015t0002g0025 others(17): 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 | 3 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0010c0009t0015g0032 |
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 | 2 | a0003c0015t0002g0025 a0003c0015t0002g0320 |
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 | a0003c0070t0002g0042 a0020c0069t0002g0041 |
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 | 18 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(15): 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 | a0001c0001t0001g0254 | 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 | a0030c0067t0001g0037 a0036c0068t0001g0038 |
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 | 3 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0010c0009t0015g0032 |
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 | a0001c0001t0001g0062 a0001c0001t0001g0073 a0001c0003t0002g0033 others(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 | a0001c0001t0001g0245 | 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 | a0034c0046t0016g0123 | 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 | a0001c0003t0002g0275 | 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 | a0002c0002t0001g0029 | 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 | a0003c0007t0008g0047 a0003c0007t0009g0007 a0003c0007t0009g0048 others(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 | 126 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(123): 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 | a0001c0001t0001g0028 | 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 | a0005c0038t0011g0057 | 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 | 127 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(124): 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 | 4 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0010c0009t0015g0032 others(1): 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 | a0001c0001t0001g0316 | 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 | 122 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(119): 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 | a0001c0001t0001g0235 | 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 | a0002c0004t0002g0175 | 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 | 5 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0010c0009t0015g0032 others(2): 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 | a0002c0002t0001g0287 | 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 | a0003c0070t0002g0042 a0020c0069t0002g0041 |
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 | a0027c0063t0001g0233 | 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 | 6 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0010c0009t0015g0032 others(3): 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 | 2 | a0003c0015t0002g0025 a0003c0015t0002g0320 |
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 | a0001c0001t0001g0150 | 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 | a0002c0004t0027g0266 | 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 | 17 | a0001c0054t0002g0220 a0002c0004t0002g0061 a0006c0010t0002g0009 others(14): 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 | 139 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(136): 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 | a0023c0066t0002g0205 | 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 | a0002c0002t0001g0174 | 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 | a0026c0026t0001g0127 | 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 | 5 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0010c0009t0015g0032 others(2): 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 | a0006c0010t0002g0011 a0028c0045t0002g0065 |
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 | a0003c0007t0008g0047 a0003c0007t0009g0007 a0003c0007t0009g0048 others(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 | 123 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(120): 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 | a0004c0005t0001g0195 | 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 | 6 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0010c0009t0015g0032 others(3): 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 | 5 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0010c0009t0015g0032 others(2): 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 | a0001c0001t0001g0014 a0001c0001t0001g0074 a0001c0001t0001g0078 others(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 | a0023c0066t0002g0205 | 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 | 1 | a0006c0010t0002g0009 | 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 | 270 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0027 others(267): Show |
294 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(291): 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 | a0002c0004t0002g0061 a0029c0042t0006g0060 |
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 | a0001c0055t0002g0214 a0014c0053t0013g0046 |
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 | 20 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(17): 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 | 26 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0125 others(23): Show |
30 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(27): 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 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
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 | a0038c0048t0001g0111 | 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 | a0002c0002t0002g0068 | 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 | a0030c0067t0001g0037 a0036c0068t0001g0038 a0043c0071t0002g0325 |
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 | a0001c0001t0001g0062 a0001c0001t0001g0073 |
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 | a0002c0004t0002g0201 | 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 | a0002c0002t0002g0039 | 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 | a0003c0070t0002g0042 a0020c0069t0002g0041 |
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 | a0001c0001t0018g0056 | 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 | a0001c0001t0001g0235 | 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 | 5 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0010c0009t0015g0032 others(2): 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 | 6 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0010c0009t0015g0032 others(3): 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 | a0002c0002t0002g0039 | 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 | 6 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0010c0009t0015g0032 others(3): 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 | 6 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0010c0009t0015g0032 others(3): 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 | a0002c0002t0001g0177 | 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 | a0023c0066t0002g0205 | 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 | 30 | a0001c0001t0001g0022 a0001c0001t0001g0028 a0001c0001t0001g0079 others(27): 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 |
1 | a0003c0015t0002g0025 | 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 | a0003c0015t0002g0320 a0010c0009t0015g0032 a0034c0046t0016g0123 |
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 | a0037c0040t0014g0045 | 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 | a0023c0066t0002g0205 | 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 | a0001c0003t0002g0147 | 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 | 6 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0010c0009t0015g0032 others(3): 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 | a0002c0031t0004g0066 | 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 | a0023c0066t0002g0205 | 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 | a0001c0001t0001g0076 | 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 | a0001c0003t0002g0285 | 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 | a0030c0067t0001g0037 a0036c0068t0001g0038 |
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 | a0038c0048t0001g0111 | 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 | a0040c0027t0001g0110 | 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 | a0038c0048t0001g0111 | 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 | a0038c0048t0001g0111 | 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 | a0005c0038t0011g0057 | 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 | a0001c0003t0002g0058 | 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 | a0010c0009t0028g0067 | 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 | 4 | a0006c0010t0002g0009 a0006c0021t0001g0008 a0019c0020t0002g0054 others(1): 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 | a0001c0055t0002g0214 a0002c0002t0008g0043 a0005c0038t0011g0057 others(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 | a0002c0002t0002g0039 | 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 | 147 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(144): 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 | a0030c0067t0001g0037 a0036c0068t0001g0038 a0043c0071t0002g0325 |
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 | a0002c0002t0001g0163 | 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 | 30 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0001g0130 others(27): 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 | a0001c0001t0001g0120 a0002c0002t0003g0121 a0020c0069t0002g0041 others(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 | 16 | a0001c0001t0001g0119 a0002c0002t0001g0017 a0002c0002t0001g0055 others(13): 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 | a0002c0002t0001g0204 a0003c0007t0009g0007 a0003c0007t0009g0048 others(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 | a0001c0001t0001g0324 a0002c0002t0001g0020 a0002c0002t0001g0155 others(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 | 7 | a0002c0004t0002g0010 a0006c0010t0002g0009 a0006c0021t0001g0008 others(4): Show |
8 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(5): 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 | 106 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(103): 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 | a0002c0002t0001g0015 a0002c0002t0001g0016 a0002c0002t0001g0113 others(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 | a0005c0038t0011g0057 | 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 | a0029c0042t0006g0060 | 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 | a0003c0007t0008g0047 a0003c0007t0009g0007 a0003c0007t0009g0048 others(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 | a0002c0013t0001g0019 a0002c0013t0021g0019 |
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 | a0013c0019t0001g0072 a0013c0019t0002g0129 a0013c0035t0002g0151 |
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 | a0002c0002t0001g0162 | 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 | 128 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(125): 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 | a0002c0002t0002g0039 | 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 | 5 | a0006c0010t0002g0009 a0006c0021t0001g0008 a0019c0020t0002g0050 others(2): 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 | 3 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0037c0040t0014g0045 |
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 | a0002c0004t0002g0146 | 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 | a0023c0066t0002g0205 a0030c0067t0001g0037 a0036c0068t0001g0038 others(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 | 154 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(151): Show |
164 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(161): 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 | a0029c0042t0006g0060 | 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 | a0002c0002t0001g0161 | 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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
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 | 1 | a0002c0004t0002g0010 | 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 | a0001c0001t0001g0302 | 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 | a0001c0003t0002g0097 | 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 | a0001c0003t0002g0097 | 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 | a0001c0003t0002g0097 | 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 | a0002c0004t0002g0200 | 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 | 10 | a0003c0007t0008g0047 a0003c0007t0009g0007 a0003c0007t0009g0048 others(7): 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 | 124 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0105 others(121): 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 | a0014c0052t0002g0248 | 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 | a0014c0051t0001g0218 | 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 | a0001c0001t0001g0311 | 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 | a0003c0070t0002g0042 | 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 | a0001c0003t0002g0275 a0008c0016t0002g0297 a0012c0022t0001g0286 |
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 | 286 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(283): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): 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 | a0002c0002t0001g0244 | 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 | 293 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(290): Show |
317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): 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 | a0001c0001t0001g0124 a0001c0001t0001g0125 |
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 | 113 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0062 others(110): 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 | a0002c0002t0001g0165 | 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 | a0002c0004t0002g0188 a0002c0004t0002g0191 a0002c0004t0002g0192 others(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 | a0005c0038t0011g0057 | 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 | a0002c0002t0001g0029 | 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 | a0003c0070t0002g0042 | 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 | a0001c0003t0002g0033 a0002c0004t0002g0188 a0002c0004t0002g0191 others(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 | a0003c0070t0002g0042 | 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 | a0001c0001t0001g0234 | 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 | a0002c0002t0002g0206 | 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 | a0002c0002t0001g0203 | 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 | a0003c0007t0009g0048 | 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 | 130 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0062 others(127): 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 | 109 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0062 others(106): 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 | a0005c0038t0011g0057 | 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 | 112 | a0001c0001t0001g0027 a0001c0001t0001g0130 a0001c0001t0001g0132 others(109): Show |
125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): 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 | a0003c0044t0002g0213 | 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 | a0029c0042t0006g0060 | 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 | a0029c0042t0006g0060 | 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 | a0001c0054t0002g0220 a0003c0036t0002g0040 a0003c0070t0002g0042 others(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 | a0001c0001t0001g0316 | 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 | a0011c0011t0001g0052 a0011c0011t0001g0107 a0011c0011t0002g0106 |
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 | a0001c0001t0001g0254 | 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 | 155 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(152): 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 | 168 | a0001c0001t0001g0256 a0001c0001t0001g0302 a0001c0001t0001g0309 others(165): Show |
192 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(189): 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 | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0126 others(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 | a0002c0002t0002g0039 | 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 | a0001c0003t0002g0096 a0001c0054t0002g0220 a0001c0055t0002g0214 others(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 | 151 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(148): 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 | a0001c0055t0002g0214 a0014c0053t0013g0046 |
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 | 311 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(308): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.681-73A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 5/18 | chr4 | 6593100 | |||||||
chr4:6593389 | C | T | 6 | a0006c0010t0002g0009 a0006c0010t0002g0011 a0019c0020t0002g0050 others(3): 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 | a0001c0001t0001g0076 | 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 | a0002c0002t0001g0015 a0002c0002t0001g0115 a0002c0004t0002g0112 |
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 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
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 | 151 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(148): 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 | a0002c0004t0002g0061 | 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 | a0001c0055t0002g0214 | 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 | a0001c0001t0001g0254 | 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 | a0002c0002t0001g0069 a0002c0002t0001g0249 |
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 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
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 | a0001c0001t0001g0130 | 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 | 171 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(168): 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 | a0023c0066t0002g0205 | 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 | a0010c0009t0002g0051 a0010c0009t0002g0221 a0010c0009t0015g0032 others(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 | a0003c0007t0008g0047 | 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 | 7 | a0006c0010t0002g0009 a0006c0010t0002g0011 a0006c0021t0001g0008 others(4): 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 | 101 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0027 others(98): 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 | a0003c0044t0002g0213 | 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 | 323 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(320): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): 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 | a0002c0004t0002g0188 a0002c0004t0002g0317 a0011c0028t0002g0053 others(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 | 140 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0005 others(137): Show |
160 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(157): 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 | a0001c0001t0001g0308 a0001c0003t0002g0313 |
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 | 176 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(173): 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 | a0003c0041t0002g0082 a0019c0020t0002g0054 a0024c0043t0026g0071 |
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 | a0011c0011t0001g0052 a0011c0011t0001g0107 a0011c0011t0002g0106 |
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 | a0002c0004t0002g0191 | 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 | 100 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0027 others(97): 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 | 323 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(320): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): 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 | a0002c0002t0002g0319 | 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 | 151 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(148): 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 | a0001c0001t0001g0307 | 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 | a0002c0002t0001g0117 | 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 | a0016c0014t0005g0185 a0016c0014t0005g0186 |
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 | a0029c0042t0006g0060 | 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 | a0012c0022t0001g0263 | 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 | a0003c0070t0002g0042 | 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 | a0001c0054t0002g0220 a0002c0002t0001g0103 |
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 | 164 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(161): 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 | a0002c0004t0002g0188 a0002c0004t0002g0317 a0011c0028t0002g0053 others(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 | 159 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(156): 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 | 9 | a0003c0036t0002g0040 a0006c0010t0002g0009 a0006c0010t0002g0011 others(6): 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 | 126 | a0002c0002t0001g0001 a0002c0002t0001g0004 a0002c0002t0001g0005 others(123): Show |
145 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(142): 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 | a0015c0012t0002g0197 | 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 | a0001c0055t0002g0214 a0014c0053t0013g0046 |
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 | 177 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(174): 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 | 24 | a0001c0055t0002g0214 a0003c0007t0008g0047 a0003c0007t0009g0007 others(21): 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 | 9 | a0003c0036t0002g0040 a0006c0010t0002g0009 a0006c0010t0002g0011 others(6): 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 | a0001c0003t0002g0275 | 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 | a0002c0002t0001g0103 a0002c0002t0001g0158 |
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 | 16 | a0001c0055t0002g0214 a0003c0007t0008g0047 a0003c0007t0009g0007 others(13): 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 | a0035c0056t0006g0219 | 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 | a0002c0002t0001g0133 | 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 | 5 | a0006c0010t0002g0009 a0006c0010t0002g0011 a0006c0021t0001g0008 others(2): 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 | a0044c0029t0001g0212 | 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 | 7 | a0006c0010t0002g0009 a0006c0010t0002g0011 a0006c0021t0001g0008 others(4): 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 | a0001c0001t0001g0100 | 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 | 8 | a0003c0036t0002g0040 a0006c0010t0002g0009 a0006c0010t0002g0011 others(5): 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 | a0001c0001t0001g0223 | 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 | 175 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(172): 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 | 26 | a0001c0054t0002g0220 a0001c0055t0002g0214 a0003c0015t0002g0025 others(23): 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 | a0001c0001t0001g0028 | 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 | a0023c0066t0002g0205 | 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 | a0008c0050t0024g0222 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0087 a0001c0003t0002g0003 others(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 | a0007c0006t0001g0075 | 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 | a0002c0002t0029g0143 | 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 | 5 | a0001c0055t0002g0214 a0003c0015t0002g0025 a0003c0015t0002g0320 others(2): 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 | a0003c0041t0002g0082 a0024c0043t0026g0071 |
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 | a0001c0054t0002g0220 a0003c0041t0002g0082 a0003c0070t0002g0042 others(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 | a0019c0020t0002g0054 | 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 | a0001c0001t0001g0277 a0041c0059t0001g0252 |
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 | a0001c0001t0001g0095 | 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 | 3 | a0003c0015t0002g0025 a0003c0015t0002g0320 a0037c0040t0014g0045 |
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 | a0001c0003t0002g0147 | 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 | a0023c0066t0002g0205 | 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 | 19 | a0001c0054t0002g0220 a0001c0055t0002g0214 a0003c0015t0002g0025 others(16): 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 | 16 | a0003c0036t0002g0040 a0006c0010t0002g0009 a0006c0010t0002g0011 others(13): 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 | 6 | a0001c0055t0002g0214 a0003c0015t0002g0025 a0003c0015t0002g0320 others(3): 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 | 20 | a0003c0007t0008g0047 a0003c0007t0009g0007 a0003c0007t0009g0048 others(17): 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 | 40 | a0001c0054t0002g0220 a0001c0055t0002g0214 a0003c0007t0008g0047 others(37): 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 | 18 | a0001c0054t0002g0220 a0001c0055t0002g0214 a0003c0015t0002g0025 others(15): 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 | 8 | a0003c0036t0002g0040 a0006c0010t0002g0009 a0006c0010t0002g0011 others(5): 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 | a0024c0043t0026g0071 | 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 | 18 | a0001c0054t0002g0220 a0001c0055t0002g0214 a0003c0015t0002g0025 others(15): 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 | a0024c0043t0026g0071 | 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 | a0001c0003t0002g0033 a0001c0003t0002g0251 a0002c0002t0001g0134 others(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 | 140 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(137): 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 | 8 | a0001c0001t0003g0243 a0001c0003t0002g0088 a0001c0003t0002g0250 others(5): 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 | a0024c0043t0026g0071 | 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 | a0001c0001t0001g0321 | 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 | a0001c0054t0002g0220 a0003c0070t0002g0042 a0008c0050t0024g0222 others(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 | a0002c0002t0001g0055 a0002c0002t0001g0117 |
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 | 183 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(180): 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 | a0001c0003t0002g0033 | 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 | 160 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(157): 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 | a0014c0052t0002g0248 | 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 | 182 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(179): 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 | a0003c0007t0008g0047 a0003c0007t0009g0007 a0003c0007t0009g0048 others(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 | a0001c0001t0001g0256 a0001c0001t0001g0302 a0001c0001t0001g0309 |
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 | a0001c0001t0001g0316 | 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 | a0001c0001t0001g0027 | 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 | a0001c0001t0001g0298 | 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 | 182 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(179): 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 | a0036c0068t0001g0038 | 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 | 182 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(179): 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 | a0001c0001t0001g0118 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0074 others(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 | a0002c0002t0001g0169 | 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 | a0010c0009t0002g0051 a0010c0009t0015g0032 a0010c0009t0028g0067 others(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 | 307 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(304): Show |
335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): 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 | a0001c0001t0001g0024 a0001c0001t0001g0322 a0001c0001t0017g0024 |
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 | a0031c0039t0006g0049 a0032c0047t0025g0183 |
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 | a0001c0003t0002g0096 | 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 | a0002c0002t0001g0158 | 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 | a0001c0001t0001g0293 | 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 | 29 | a0001c0003t0002g0059 a0001c0054t0002g0220 a0002c0032t0010g0030 others(26): 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 | a0001c0001t0001g0255 a0001c0001t0001g0258 a0001c0001t0003g0243 others(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 | 97 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0027 others(94): 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 | 13 | a0006c0010t0002g0009 a0006c0010t0002g0011 a0006c0021t0001g0008 others(10): 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 | a0002c0002t0001g0023 | 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 | a0005c0038t0011g0057 | 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 | a0020c0037t0002g0207 | 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 | a0001c0003t0002g0147 | 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 | a0001c0001t0001g0211 | 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 | 52 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0074 others(49): 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 | 181 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(178): 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 | a0003c0036t0002g0040 a0003c0070t0002g0042 a0016c0014t0005g0184 others(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 | 181 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(178): 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 | a0001c0001t0001g0024 a0001c0001t0001g0322 a0001c0001t0017g0024 |
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 | 22 | a0001c0054t0002g0220 a0003c0007t0008g0047 a0003c0007t0009g0007 others(19): 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 | 177 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(174): 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 | a0001c0003t0002g0033 | 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 | a0007c0006t0001g0144 | 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 | a0005c0038t0011g0057 a0019c0020t0002g0054 a0023c0066t0002g0205 others(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 | a0016c0014t0005g0186 | 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 | a0034c0046t0016g0123 | 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 | a0020c0037t0002g0207 | 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 | a0003c0007t0008g0047 a0003c0007t0009g0007 a0003c0007t0009g0048 others(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 | a0010c0009t0002g0051 | 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 | 315 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(312): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.1540-1196A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 10/18 | chr4 | 6603859 | |||||||
chr4:6603991 | T | C | 305 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(302): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): 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 | a0002c0002t0001g0154 a0002c0004t0002g0146 |
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 | a0001c0003t0002g0147 | 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 | a0001c0003t0002g0187 | 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 | a0001c0001t0001g0080 a0001c0001t0001g0081 |
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 | a0001c0001t0001g0298 | 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 | a0001c0003t0002g0187 | 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 | 103 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0027 others(100): 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 | a0002c0004t0002g0175 | 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 | a0001c0054t0002g0220 a0035c0056t0006g0219 |
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 | 6 | a0002c0002t0001g0017 a0002c0002t0001g0055 a0002c0002t0001g0116 others(3): 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 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0074 others(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 | a0001c0001t0001g0119 | 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 | a0014c0053t0013g0046 | 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 | a0031c0039t0006g0049 | 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 | 5 | a0006c0010t0002g0009 a0006c0010t0002g0011 a0006c0021t0001g0008 others(2): 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 | 50 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0074 others(47): 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 | a0002c0002t0001g0323 a0021c0018t0001g0026 a0021c0018t0020g0026 |
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 | a0003c0044t0002g0213 | 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 | a0002c0002t0002g0319 | 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 | 170 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(167): 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 | a0001c0001t0001g0229 a0001c0001t0001g0273 |
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 | a0001c0055t0002g0214 a0003c0041t0002g0082 |
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 | 166 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(163): 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 | 71 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0074 others(68): 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 | a0002c0002t0001g0172 | 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 | a0007c0006t0001g0063 a0007c0006t0001g0075 |
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 | a0001c0001t0003g0281 | 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 | a0006c0021t0001g0008 | 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 | 32 | a0002c0002t0001g0004 a0002c0002t0001g0005 a0002c0002t0001g0035 others(29): Show |
36 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(33): 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 | a0001c0001t0003g0271 | 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 | a0002c0002t0001g0158 | 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 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0074 others(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 | 115 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0027 others(112): 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 | a0010c0009t0002g0051 a0010c0009t0002g0221 a0010c0009t0015g0032 others(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 | a0002c0002t0008g0031 a0011c0011t0001g0052 a0011c0011t0001g0107 others(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 | a0001c0001t0001g0118 | 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 | a0031c0039t0006g0049 | 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 | a0014c0053t0013g0046 | 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 | 198 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(195): 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 | a0001c0001t0001g0122 | 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 | a0010c0009t0002g0051 a0010c0009t0002g0221 a0010c0009t0015g0032 others(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 | a0001c0003t0002g0267 | 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 | a0003c0044t0002g0213 | 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 | a0002c0002t0001g0169 | 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 | a0001c0054t0002g0220 a0003c0007t0008g0047 a0003c0007t0009g0007 others(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 | a0002c0013t0001g0019 a0002c0013t0021g0019 a0041c0059t0001g0252 |
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 | a0002c0002t0001g0117 | 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 | 43 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0074 others(40): 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 | a0010c0009t0028g0067 | 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 | 106 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0027 others(103): 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 | 109 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0027 others(106): 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 | a0002c0002t0001g0128 a0026c0026t0001g0127 |
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 | a0024c0043t0026g0071 | 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 | 61 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0074 others(58): 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 | a0001c0055t0002g0214 a0003c0041t0002g0082 a0003c0070t0002g0042 others(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 | 43 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0074 others(40): 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 | a0003c0007t0008g0047 a0003c0007t0009g0007 a0003c0007t0009g0048 others(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 | a0001c0001t0001g0231 a0001c0001t0001g0291 |
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 | 69 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0074 others(66): 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 | a0032c0047t0025g0183 | 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 | a0007c0006t0001g0173 | 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 | a0002c0002t0001g0155 | 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 | a0001c0001t0001g0090 a0001c0003t0002g0096 |
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 | 85 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0074 others(82): 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 | a0010c0009t0002g0051 a0010c0009t0002g0221 a0010c0009t0015g0032 others(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 | a0002c0031t0004g0066 | 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 | a0035c0056t0006g0219 | 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 | a0001c0001t0001g0119 | 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 | a0002c0002t0001g0085 a0002c0002t0001g0108 |
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 | 81 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0074 others(78): 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 | a0001c0054t0002g0220 a0003c0044t0002g0213 a0019c0020t0002g0050 others(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 | a0002c0002t0001g0170 | 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 | a0019c0020t0002g0050 a0024c0043t0026g0071 |
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 | a0014c0051t0001g0218 a0014c0052t0002g0248 a0014c0053t0013g0046 others(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 | a0001c0001t0001g0254 a0010c0009t0002g0051 a0010c0009t0002g0221 others(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 | a0002c0013t0001g0019 a0002c0013t0021g0019 a0003c0007t0008g0047 others(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 | a0032c0047t0025g0183 | 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 | a0003c0007t0008g0047 a0003c0007t0009g0007 a0003c0007t0009g0048 others(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 | a0001c0001t0001g0027 | 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 | 90 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0074 others(87): 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 | a0014c0053t0013g0046 | 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 | a0023c0066t0002g0205 | 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 | a0014c0051t0001g0218 | 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 | a0003c0007t0009g0007 | 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 | a0003c0007t0008g0047 | 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 | a0003c0007t0012g0070 a0014c0052t0002g0248 |
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 | a0003c0007t0009g0048 | 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 | a0002c0002t0001g0140 | 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 | a0001c0001t0001g0294 | 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 | 65 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0074 others(62): 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 | a0001c0054t0002g0220 a0003c0044t0002g0213 a0019c0020t0002g0050 others(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 | a0002c0002t0001g0006 a0002c0002t0001g0287 a0002c0002t0001g0288 others(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 | 96 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0074 others(93): 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 | a0003c0007t0008g0047 a0003c0007t0009g0007 a0003c0007t0009g0048 others(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 | a0003c0007t0008g0047 a0003c0007t0009g0007 a0003c0007t0009g0048 others(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 | a0032c0047t0025g0183 | 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 | a0001c0001t0001g0254 a0010c0009t0002g0051 a0010c0009t0002g0221 others(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 | 95 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0074 others(92): 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 | a0032c0047t0025g0183 | 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 | a0003c0070t0002g0042 a0008c0016t0005g0208 a0016c0014t0005g0184 others(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 | a0031c0039t0006g0049 | 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 | a0001c0001t0001g0254 a0010c0009t0002g0051 a0010c0009t0002g0221 others(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 | a0001c0001t0001g0254 a0010c0009t0002g0051 a0010c0009t0002g0221 others(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 | a0001c0054t0002g0220 a0003c0044t0002g0213 a0019c0020t0002g0050 others(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 | 74 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0074 others(71): 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 | a0001c0001t0001g0254 a0010c0009t0002g0051 a0010c0009t0002g0221 others(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 | 59 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0074 others(56): 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 | a0010c0009t0002g0051 a0010c0009t0002g0221 a0010c0009t0015g0032 others(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 | a0014c0051t0001g0218 a0023c0066t0002g0205 |
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 | a0003c0041t0002g0082 a0003c0070t0002g0042 a0008c0016t0005g0208 others(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 | a0014c0051t0001g0218 | 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 | a0001c0001t0001g0293 | 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 | a0001c0003t0002g0168 | 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 | a0014c0053t0013g0046 | 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 | a0034c0046t0016g0123 | 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 | a0001c0001t0001g0254 a0010c0009t0002g0051 a0010c0009t0002g0221 others(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 | 27 | a0001c0001t0001g0150 a0001c0001t0001g0295 a0002c0002t0001g0006 others(24): 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 | a0001c0054t0002g0220 a0003c0044t0002g0213 a0014c0051t0001g0218 others(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 | a0001c0001t0001g0078 | 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 | 141 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0091 others(138): 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 | 61 | a0001c0001t0001g0014 a0001c0001t0001g0028 a0001c0001t0001g0074 others(58): 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 | a0014c0053t0013g0046 a0031c0039t0006g0049 |
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 | a0002c0004t0002g0175 | 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 | a0014c0053t0013g0046 a0019c0020t0002g0050 a0032c0047t0025g0183 |
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 | a0032c0047t0025g0183 | 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 | a0003c0007t0009g0048 | 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 | a0010c0009t0002g0051 a0010c0009t0002g0221 a0010c0009t0028g0067 others(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 | 59 | a0001c0001t0001g0125 a0001c0001t0001g0211 a0001c0001t0001g0254 others(56): 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 | a0002c0002t0002g0319 | 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 | a0002c0004t0010g0044 | 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 | a0001c0001t0001g0093 a0001c0001t0001g0274 a0001c0003t0002g0003 others(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 | 154 | a0001c0001t0001g0024 a0001c0001t0001g0078 a0001c0001t0001g0087 others(151): 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 | a0002c0002t0001g0174 | 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 | a0010c0009t0002g0051 a0010c0009t0002g0221 a0010c0009t0028g0067 others(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 | 211 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0027 others(208): Show |
230 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(227): Show |
intron_variant | MODIFIER | c.2701+853C>T | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6615208 | |||||||
chr4:6615221 | T | C | 212 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0027 others(209): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): 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 | a0002c0004t0027g0266 a0002c0032t0010g0030 a0003c0044t0002g0213 others(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 | 111 | a0001c0001t0001g0024 a0001c0001t0001g0078 a0001c0001t0001g0087 others(108): 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 | a0002c0002t0001g0023 | 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 | 16 | a0001c0054t0002g0220 a0002c0002t0002g0039 a0002c0002t0002g0068 others(13): 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 | 107 | a0001c0001t0001g0024 a0001c0001t0001g0078 a0001c0001t0001g0087 others(104): 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 | a0001c0003t0002g0267 | 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 | a0008c0016t0005g0208 a0016c0014t0005g0184 a0016c0014t0005g0185 others(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 | a0002c0004t0027g0266 a0002c0032t0010g0030 a0003c0044t0002g0213 others(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 | a0002c0002t0001g0069 | 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 | a0002c0004t0027g0266 a0002c0032t0010g0030 a0003c0044t0002g0213 others(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 | a0007c0006t0001g0141 | 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 | a0002c0004t0027g0266 a0002c0032t0010g0030 a0003c0044t0002g0213 others(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 | a0032c0047t0025g0183 | 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 | a0002c0004t0027g0266 a0003c0044t0002g0213 a0009c0017t0002g0268 others(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 | 145 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0027 others(142): Show |
161 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(158): 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 | a0002c0002t0001g0270 | 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 | a0002c0004t0027g0266 a0002c0032t0010g0030 a0003c0044t0002g0213 others(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 | a0030c0067t0001g0037 | 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 | a0001c0001t0003g0305 a0032c0047t0025g0183 |
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 | a0002c0004t0027g0266 a0002c0032t0010g0030 a0003c0044t0002g0213 others(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 | a0002c0004t0002g0175 a0002c0004t0027g0266 a0002c0032t0010g0030 others(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 | a0008c0016t0005g0208 a0016c0014t0005g0184 a0016c0014t0005g0185 others(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 | a0002c0002t0001g0085 a0002c0002t0001g0108 |
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 | a0002c0004t0027g0266 a0002c0032t0010g0030 a0003c0044t0002g0213 others(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 | a0037c0040t0014g0045 | 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 | a0001c0001t0001g0211 | 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 | a0032c0047t0025g0183 a0033c0058t0006g0210 |
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 | a0002c0032t0010g0030 a0019c0020t0002g0050 a0024c0043t0026g0071 |
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 | a0001c0003t0002g0251 | 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 | a0008c0050t0024g0222 | 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 | a0002c0002t0001g0069 | 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 | a0002c0004t0027g0266 a0002c0032t0010g0030 a0003c0044t0002g0213 others(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 | a0002c0033t0001g0135 | 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 | a0023c0066t0002g0205 | 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 | 22 | a0001c0054t0002g0220 a0002c0002t0002g0039 a0002c0002t0002g0068 others(19): 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 | a0008c0016t0005g0208 a0016c0014t0005g0184 a0016c0014t0005g0185 others(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 | a0002c0004t0002g0188 a0002c0004t0002g0317 a0011c0028t0002g0053 |
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 | 279 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(276): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.2702-103A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 16/18 | chr4 | 6617277 | |||||||
chr4:6617325 | A | G | 274 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(271): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(295): 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 | a0001c0003t0002g0003 a0001c0003t0002g0033 a0001c0003t0002g0058 others(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 | a0001c0001t0001g0284 | 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 | a0002c0032t0010g0030 a0019c0020t0002g0050 a0024c0043t0026g0071 |
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 | a0001c0003t0002g0003 a0001c0003t0002g0033 a0001c0003t0002g0058 others(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 | a0001c0003t0002g0003 a0001c0003t0002g0033 a0001c0003t0002g0058 others(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 | 22 | a0001c0001t0001g0090 a0001c0054t0002g0220 a0002c0002t0001g0134 others(19): 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 | 219 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0027 others(216): Show |
240 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(237): 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 | a0001c0001t0001g0024 a0001c0001t0001g0073 a0001c0001t0001g0234 others(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 | a0008c0016t0002g0209 | 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 | a0001c0003t0002g0003 a0001c0003t0002g0033 a0001c0003t0002g0058 others(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 | a0002c0002t0001g0138 | 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 | a0019c0020t0002g0054 | 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 | a0008c0050t0024g0222 | 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 | 27 | a0001c0003t0002g0267 a0001c0003t0002g0285 a0002c0004t0002g0010 others(24): 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 | 44 | a0001c0003t0002g0267 a0001c0003t0002g0285 a0001c0054t0002g0220 others(41): 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 | a0002c0002t0001g0154 | 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 | a0001c0001t0001g0282 | 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 | a0002c0002t0008g0031 a0011c0011t0001g0052 a0011c0011t0001g0107 |
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 | a0002c0002t0001g0171 | 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 | a0002c0002t0001g0055 | 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 | a0005c0008t0004g0012 | 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 | a0033c0058t0006g0210 | 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 | a0001c0001t0001g0105 | 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 | a0002c0002t0001g0085 a0002c0002t0001g0108 |
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 | a0011c0011t0001g0052 | 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 | a0002c0032t0010g0030 a0019c0020t0002g0050 a0024c0043t0026g0071 |
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 | a0001c0001t0003g0271 | 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 | 18 | a0001c0054t0002g0220 a0002c0002t0002g0039 a0002c0002t0002g0068 others(15): 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 | 26 | a0001c0003t0002g0267 a0001c0003t0002g0285 a0002c0004t0002g0010 others(23): 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 | 14 | a0001c0054t0002g0220 a0002c0002t0002g0039 a0002c0002t0002g0068 others(11): 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 | a0019c0020t0002g0054 | 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 | a0008c0016t0002g0297 a0012c0049t0002g0101 |
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 | a0008c0016t0005g0208 a0016c0014t0005g0184 a0016c0014t0005g0185 others(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 | 224 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(221): Show |
246 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(243): 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 | a0023c0066t0002g0205 | 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 | 281 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(278): Show |
308 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(305): 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 | a0001c0001t0001g0311 | 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 | a0001c0001t0001g0255 a0002c0002t0001g0260 |
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 | a0015c0012t0002g0197 | 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 | 323 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(320): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.2815-663A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6619264 | |||||||
chr4:6619370 | A | G | 327 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(324): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): Show |
intron_variant | MODIFIER | c.2815-557A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6619370 | |||||||
chr4:6619377 | A | G | 318 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(315): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.2815-550A>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 17/18 | chr4 | 6619377 | |||||||
chr4:6619461 | G | C | 289 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(286): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): 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 | a0008c0050t0024g0222 a0032c0047t0025g0183 |
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 | a0029c0042t0006g0060 a0031c0039t0006g0049 a0033c0058t0006g0210 others(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 | a0002c0004t0007g0178 | 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 | a0043c0071t0002g0325 | 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 | a0001c0054t0002g0220 a0002c0002t0002g0068 a0002c0002t0002g0206 others(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 | a0028c0045t0002g0065 | 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 | a0003c0036t0002g0040 a0020c0037t0002g0207 a0020c0069t0002g0041 |
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 | a0001c0001t0001g0279 a0001c0001t0001g0315 |
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 | a0008c0016t0002g0209 | 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 | 327 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(324): Show |
356 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(353): 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 | a0002c0004t0002g0061 a0002c0004t0002g0188 a0002c0004t0002g0191 others(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 | a0008c0016t0005g0208 a0016c0014t0005g0184 a0016c0014t0005g0185 others(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 | a0001c0003t0002g0003 a0001c0003t0002g0033 a0001c0003t0002g0058 others(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 | 323 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(320): Show |
352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.2932+400C>G | MAN2B2 | ENSG00000013288.9 | transcript | ENST00000285599.8 | protein_coding | 18/18 | chr4 | 6620444 | |||||||
chr4:6620454 | G | A | 14 | a0001c0054t0002g0220 a0002c0002t0002g0039 a0002c0002t0002g0068 others(11): 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 | a0002c0002t0001g0323 | 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 | a0008c0016t0005g0208 a0016c0014t0005g0184 a0016c0014t0005g0185 others(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 | 318 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(315): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): 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 | a0002c0002t0001g0137 | 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 | a0008c0050t0024g0222 a0032c0047t0025g0183 |
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 | a0002c0002t0001g0139 | 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 | a0001c0001t0001g0081 | 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 | a0001c0001t0001g0224 | 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 | 318 | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0024 others(315): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): 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 | a0001c0001t0001g0293 | 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 | 29 | a0001c0003t0002g0267 a0001c0003t0002g0285 a0002c0002t0001g0117 others(26): 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 | a0002c0004t0002g0061 a0002c0004t0002g0188 a0002c0004t0002g0191 others(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 |