Item | Value |
---|---|
geneid | 11253 |
ensemblid | ENSG00000177239.16 |
hgncid | 6823 |
symbol | MAN1B1 |
name | mannosidase alpha class 1B member 1 |
refseq_nuc | NM_016219.5 |
refseq_prot | NP_057303.2 |
ensembl_nuc | ENST00000371589.9 |
ensembl_prot | ENSP00000360645.4 |
mane_status | MANE Select |
chr | chr9 |
start | 137086985 |
end | 137109183 |
strand | + |
ver | v1.2 |
region | chr9:137086985-137109183 |
region5000 | chr9:137081985-137114183 |
regionname0 | MAN1B1_chr9_137086985_137109183 |
regionname5000 | MAN1B1_chr9_137081985_137114183 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 699 | 340 | 51 | 68 | 161 | 17 | 43 | 122 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | MAACE others(694): Show |
chr9 | 137081985 | 137114183 |
a0002 | 0/0 | 699 | 33 | 31 | 1 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | MAACE others(694): Show |
chr9 | 137081985 | 137114183 |
a0003 | 0/0 | 699 | 9 | 0 | 8 | 0 | 0 | 1 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | MAACE others(694): Show |
chr9 | 137081985 | 137114183 |
a0004 | 0/0 | 699 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | MAACE others(694): Show |
chr9 | 137081985 | 137114183 |
a0005 | 0/0 | 699 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | MAACE others(694): Show |
chr9 | 137081985 | 137114183 |
a0006 | 0/0 | 699 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | MAACE others(694): Show |
chr9 | 137081985 | 137114183 |
a0007 | 0/0 | 699 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | MAACE others(694): Show |
chr9 | 137081985 | 137114183 |
a0008 | 0/0 | 699 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | MAACE others(694): Show |
chr9 | 137081985 | 137114183 |
a0009 | 0/0 | 699 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | MAACE others(694): Show |
chr9 | 137081985 | 137114183 |
a0010 | 0/0 | 699 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | MAACE others(694): Show |
chr9 | 137081985 | 137114183 |
a0011 | 0/0 | 699 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | MAACE others(694): Show |
chr9 | 137081985 | 137114183 |
a0012 | 0/0 | 699 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | MAACE others(694): Show |
chr9 | 137081985 | 137114183 |
a0013 | 0/0 | 699 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | MAACE others(694): Show |
chr9 | 137081985 | 137114183 |
a0014 | 0/0 | 699 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | MAACE others(694): Show |
chr9 | 137081985 | 137114183 |
a0015 | 0/0 | 699 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | MAACE others(694): Show |
chr9 | 137081985 | 137114183 |
a0016 | 0/0 | 699 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | MAACE others(694): Show |
chr9 | 137081985 | 137114183 |
a0017 | 0/0 | 699 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | MAACE others(694): Show |
chr9 | 137081985 | 137114183 |
a0018 | 0/0 | 699 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | MAACE others(694): Show |
chr9 | 137081985 | 137114183 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2097 | 247 | 47 | 43 | 108 | 14 | 35 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0001c0002 | 0/0 | 2097 | 79 | 1 | 17 | 52 | 3 | 6 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0001c0005 | 0/0 | 2097 | 6 | 0 | 5 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0001c0007 | 0/0 | 2097 | 3 | 2 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0001c0017 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0001c0022 | 0/0 | 2097 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0001c0023 | 0/0 | 2097 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0001c0025 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0001c0029 | 0/0 | 2097 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0002c0003 | 0/0 | 2097 | 30 | 28 | 1 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0002c0009 | 0/0 | 2097 | 2 | 2 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0002c0012 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0003c0004 | 0/0 | 2097 | 9 | 0 | 8 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0004c0006 | 0/0 | 2097 | 4 | 4 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0005c0008 | 0/0 | 2097 | 2 | 2 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0005c0013 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0006c0011 | 0/0 | 2097 | 2 | 0 | 0 | 2 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0007c0010 | 0/0 | 2097 | 2 | 0 | 0 | 2 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0008c0016 | 0/0 | 2097 | 1 | 0 | 0 | 0 | 1 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0009c0014 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0010c0018 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0011c0021 | 0/0 | 2097 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0012c0020 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0013c0019 | 0/0 | 2097 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0014c0015 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0015c0026 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0016c0028 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0017c0027 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 | ||
a0018c0024 | 0/0 | 2097 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | ATGGC others(2092): Show |
chr9 | 137081985 | 137114183 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2707 | 178 | 33 | 27 | 97 | 4 | 17 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0001c0001t0002 | 0/0 | 2707 | 36 | 5 | 12 | 1 | 8 | 10 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0001c0001t0003 | 0/0 | 2708 | 21 | 1 | 4 | 6 | 2 | 8 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2703): Show |
chr9 | 137081985 | 137114183 |
a0001c0001t0005 | 0/0 | 2707 | 6 | 6 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0001c0001t0006 | 0/0 | 2707 | 4 | 0 | 0 | 4 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0001c0001t0007 | 0/0 | 2707 | 2 | 2 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0001c0002t0001 | 0/0 | 2707 | 4 | 0 | 0 | 3 | 1 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0001c0002t0002 | 0/0 | 2707 | 74 | 1 | 17 | 49 | 2 | 5 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0001c0002t0004 | 0/0 | 2708 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2703): Show |
chr9 | 137081985 | 137114183 |
a0001c0005t0002 | 0/0 | 2707 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0001c0005t0004 | 0/0 | 2708 | 5 | 0 | 4 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2703): Show |
chr9 | 137081985 | 137114183 |
a0001c0007t0001 | 0/0 | 2707 | 3 | 2 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0001c0017t0001 | 0/0 | 2707 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0001c0022t0001 | 0/0 | 2707 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0001c0023t0001 | 0/0 | 2707 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0001c0025t0001 | 0/0 | 2707 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0001c0029t0001 | 0/0 | 2707 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0002c0003t0001 | 0/0 | 2707 | 6 | 6 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0002c0003t0002 | 0/0 | 2707 | 24 | 22 | 1 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0002c0009t0002 | 0/0 | 2707 | 2 | 2 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0002c0012t0002 | 0/0 | 2707 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0003c0004t0001 | 0/0 | 2707 | 9 | 0 | 8 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0004c0006t0001 | 0/0 | 2707 | 4 | 4 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0005c0008t0002 | 0/0 | 2707 | 2 | 2 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0005c0013t0002 | 0/0 | 2707 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0006c0011t0002 | 0/0 | 2707 | 2 | 0 | 0 | 2 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0007c0010t0002 | 0/0 | 2707 | 2 | 0 | 0 | 2 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0008c0016t0002 | 0/0 | 2707 | 1 | 0 | 0 | 0 | 1 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0009c0014t0002 | 0/0 | 2707 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0010c0018t0002 | 0/0 | 2707 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0011c0021t0002 | 0/0 | 2707 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0012c0020t0001 | 0/0 | 2707 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0013c0019t0002 | 0/0 | 2707 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0014c0015t0001 | 0/0 | 2707 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0015c0026t0001 | 0/0 | 2707 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0016c0028t0002 | 0/0 | 2707 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0017c0027t0002 | 0/0 | 2707 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
a0018c0024t0001 | 0/0 | 2707 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | GTTGA others(2702): Show |
chr9 | 137081985 | 137114183 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 18 | 4 | 3 | 7 | 0 | 4 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0002 | 0/0 | 20 | 0 | 3 | 15 | 0 | 2 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0005 | 0/0 | 9 | 3 | 0 | 5 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0010 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0014 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 0 | 2 | 2 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0018 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0023 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0045 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0047 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0013 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0015 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0034 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0038 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0003g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0003g0004 | 0/0 | 9 | 0 | 2 | 3 | 1 | 3 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0003g0048 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0003g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0005g0012 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0005g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0006g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0006g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0007g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0003 | 0/0 | 17 | 0 | 4 | 13 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0007 | 0/0 | 7 | 0 | 3 | 1 | 1 | 2 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0009 | 0/0 | 6 | 1 | 4 | 0 | 1 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0011 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0002t0004g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0005t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0005t0004g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0005t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0005t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0005t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0005t0004g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0007t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0007t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0007t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0017t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0022t0001g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0023t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0025t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0001c0029t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0002c0003t0001g0021 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0002c0003t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0002c0003t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0002c0003t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0002c0003t0002g0008 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0002c0003t0002g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0002c0003t0002g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0002c0003t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0002c0003t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0002c0003t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0002c0003t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0002c0003t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0002c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0002c0003t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0002c0003t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0002c0003t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0002c0003t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0002c0003t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0002c0009t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0002c0009t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0002c0012t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0003c0004t0001g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0003c0004t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0003c0004t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0003c0004t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0003c0004t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0004c0006t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0004c0006t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0005c0008t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0005c0008t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0005c0013t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0006c0011t0002g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0007c0010t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0008c0016t0002g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0009c0014t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0010c0018t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0011c0021t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0012c0020t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0013c0019t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0014c0015t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0015c0026t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0016c0028t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0017c0027t0002g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
a0018c0024t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0047 | EUR | GBR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00099 | hp2 | a0001 | c0002 | t0002 | g0007 | EUR | GBR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0124 | EUR | GBR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00140 | hp2 | a0008 | c0016 | t0002 | g0126 | EUR | GBR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0004 | EUR | FIN | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | FIN | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0057 | EUR | FIN | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | CHS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00423 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | CHS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00558 | hp2 | a0009 | c0014 | t0002 | g0082 | EAS | CHS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CHS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0079 | EAS | CHS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00621 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | CHS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00642 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00642 | hp2 | a0001 | c0005 | t0004 | g0119 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | CHS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00673 | hp2 | a0010 | c0018 | t0002 | g0058 | EAS | CHS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00733 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0146 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01070 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01071 | hp1 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01074 | hp1 | a0001 | c0007 | t0001 | g0212 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01074 | hp2 | a0001 | c0005 | t0004 | g0122 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01081 | hp2 | a0001 | c0002 | t0002 | g0078 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01106 | hp2 | a0001 | c0002 | t0002 | g0009 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01109 | hp2 | a0003 | c0004 | t0001 | g0206 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01167 | hp1 | a0001 | c0002 | t0002 | g0060 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01167 | hp2 | a0001 | c0005 | t0004 | g0013 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0011 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01175 | hp1 | a0001 | c0005 | t0004 | g0120 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01175 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01192 | hp1 | a0001 | c0023 | t0001 | g0182 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01192 | hp2 | a0001 | c0002 | t0002 | g0086 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01243 | hp2 | a0002 | c0003 | t0002 | g0107 | AMR | PUR | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01257 | hp1 | a0003 | c0004 | t0001 | g0001 | AMR | CLM | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01258 | hp1 | a0001 | c0022 | t0001 | g0001 | AMR | CLM | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01258 | hp2 | a0003 | c0004 | t0001 | g0001 | AMR | CLM | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | CLM | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0004 | AMR | CLM | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0015 | AMR | CLM | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01433 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | CLM | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0053 | AMR | CLM | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0049 | AMR | CLM | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0048 | EUR | IBS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0036 | EUR | IBS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0009 | EUR | IBS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0034 | EUR | IBS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0036 | EUR | IBS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0034 | EUR | IBS | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01884 | hp1 | a0002 | c0003 | t0001 | g0021 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01891 | hp1 | a0002 | c0009 | t0002 | g0104 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01891 | hp2 | a0002 | c0003 | t0002 | g0108 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PEL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0210 | AMR | PEL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01934 | hp2 | a0003 | c0004 | t0001 | g0001 | AMR | PEL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01943 | hp1 | a0011 | c0021 | t0002 | g0061 | AMR | PEL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01943 | hp2 | a0003 | c0004 | t0001 | g0136 | AMR | PEL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01952 | hp1 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01978 | hp1 | a0001 | c0005 | t0002 | g0013 | AMR | PEL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01978 | hp2 | a0003 | c0004 | t0001 | g0001 | AMR | PEL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01981 | hp1 | a0003 | c0004 | t0001 | g0001 | AMR | PEL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01981 | hp2 | a0003 | c0004 | t0001 | g0142 | AMR | PEL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0028 | AMR | PEL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01993 | hp2 | a0001 | c0002 | t0002 | g0007 | AMR | PEL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02040 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02055 | hp1 | a0002 | c0003 | t0001 | g0021 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02055 | hp2 | a0002 | c0012 | t0002 | g0098 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02056 | hp1 | a0002 | c0003 | t0002 | g0103 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0085 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02071 | hp1 | a0012 | c0020 | t0001 | g0016 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02083 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02129 | hp1 | a0013 | c0019 | t0002 | g0003 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0048 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02132 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0090 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02135 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02165 | hp1 | a0001 | c0002 | t0002 | g0065 | EAS | CDX | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CDX | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0110 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02273 | hp2 | a0001 | c0002 | t0002 | g0003 | AMR | PEL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02280 | hp1 | a0002 | c0003 | t0002 | g0102 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02280 | hp2 | a0002 | c0009 | t0002 | g0105 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02293 | hp1 | a0001 | c0002 | t0002 | g0031 | AMR | PEL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0013 | AMR | PEL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02300 | hp1 | a0001 | c0002 | t0002 | g0011 | AMR | PEL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0117 | AMR | PEL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02451 | hp1 | a0002 | c0003 | t0001 | g0094 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02523 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02572 | hp1 | a0002 | c0003 | t0002 | g0019 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0148 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0027 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02615 | hp1 | a0002 | c0003 | t0002 | g0008 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02630 | hp1 | a0005 | c0013 | t0002 | g0096 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0221 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02647 | hp2 | a0001 | c0007 | t0001 | g0215 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02698 | hp1 | a0001 | c0005 | t0004 | g0118 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02698 | hp2 | a0001 | c0029 | t0001 | g0001 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02717 | hp1 | a0004 | c0006 | t0001 | g0150 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02723 | hp1 | a0002 | c0003 | t0002 | g0019 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02735 | hp2 | a0001 | c0002 | t0002 | g0007 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02809 | hp2 | a0001 | c0001 | t0005 | g0113 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02818 | hp1 | a0014 | c0015 | t0001 | g0004 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02886 | hp2 | a0004 | c0006 | t0001 | g0024 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02896 | hp1 | a0002 | c0003 | t0002 | g0008 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02896 | hp2 | a0015 | c0026 | t0001 | g0151 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02897 | hp1 | a0002 | c0003 | t0002 | g0008 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02922 | hp1 | a0002 | c0003 | t0002 | g0008 | AFR | ESN | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02922 | hp2 | a0002 | c0003 | t0001 | g0021 | AFR | ESN | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02965 | hp1 | a0002 | c0003 | t0002 | g0008 | AFR | ESN | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02965 | hp2 | a0002 | c0003 | t0002 | g0100 | AFR | ESN | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02970 | hp1 | a0002 | c0003 | t0002 | g0099 | AFR | ESN | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02970 | hp2 | a0002 | c0003 | t0002 | g0020 | AFR | ESN | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02976 | hp2 | a0001 | c0007 | t0001 | g0211 | AFR | ESN | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0125 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0143 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03041 | hp1 | a0001 | c0001 | t0007 | g0154 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03098 | hp2 | a0004 | c0006 | t0001 | g0024 | AFR | MSL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03130 | hp2 | a0002 | c0003 | t0002 | g0091 | AFR | ESN | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03139 | hp1 | a0002 | c0003 | t0002 | g0106 | AFR | ESN | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | ESN | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03225 | hp2 | a0016 | c0028 | t0002 | g0129 | AFR | MSL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03239 | hp1 | a0001 | c0002 | t0002 | g0007 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | MSL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | MSL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03486 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | MSL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03516 | hp1 | a0002 | c0003 | t0001 | g0095 | AFR | ESN | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03516 | hp2 | a0005 | c0008 | t0002 | g0093 | AFR | ESN | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03579 | hp1 | a0002 | c0003 | t0002 | g0020 | AFR | MSL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | MSL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0121 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | STU | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03704 | hp1 | a0001 | c0002 | t0004 | g0059 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0055 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0069 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03831 | hp1 | a0001 | c0002 | t0002 | g0087 | SAS | BEB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0223 | SAS | BEB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0144 | SAS | BEB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03927 | hp2 | a0001 | c0002 | t0002 | g0073 | SAS | BEB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0127 | SAS | BEB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | BEB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0004 | SAS | STU | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | BEB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | STU | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0001 | SAS | STU | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | STU | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | STU | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18522 | hp2 | a0001 | c0001 | t0007 | g0155 | AFR | YRI | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18612 | hp2 | a0001 | c0002 | t0002 | g0080 | EAS | CHB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18906 | hp1 | a0002 | c0003 | t0002 | g0019 | AFR | YRI | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18906 | hp2 | a0002 | c0003 | t0002 | g0092 | AFR | YRI | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18942 | hp1 | a0001 | c0017 | t0001 | g0159 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18942 | hp2 | a0001 | c0002 | t0002 | g0077 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18943 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18947 | hp1 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18949 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18951 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18953 | hp2 | a0001 | c0002 | t0002 | g0071 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18954 | hp1 | a0001 | c0002 | t0002 | g0031 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0156 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18957 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18959 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0003 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18961 | hp1 | a0001 | c0002 | t0002 | g0084 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18964 | hp2 | a0001 | c0002 | t0002 | g0011 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18965 | hp1 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18967 | hp2 | a0001 | c0002 | t0002 | g0007 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18969 | hp1 | a0001 | c0001 | t0006 | g0180 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18970 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18974 | hp1 | a0001 | c0002 | t0002 | g0068 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18977 | hp2 | a0001 | c0002 | t0002 | g0062 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18978 | hp2 | a0006 | c0011 | t0002 | g0039 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18980 | hp2 | a0007 | c0010 | t0002 | g0001 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18981 | hp1 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18981 | hp2 | a0001 | c0002 | t0002 | g0006 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18983 | hp1 | a0001 | c0002 | t0002 | g0089 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18984 | hp1 | a0007 | c0010 | t0002 | g0001 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18984 | hp2 | a0001 | c0002 | t0002 | g0076 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18988 | hp2 | a0001 | c0002 | t0002 | g0074 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18992 | hp2 | a0001 | c0002 | t0002 | g0067 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18994 | hp1 | a0001 | c0002 | t0002 | g0075 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA18997 | hp2 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19000 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19004 | hp2 | a0001 | c0002 | t0002 | g0030 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19009 | hp1 | a0001 | c0002 | t0002 | g0051 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19009 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0123 | AFR | LWK | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19030 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | LWK | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19043 | hp1 | a0002 | c0003 | t0002 | g0020 | AFR | LWK | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19043 | hp2 | a0005 | c0008 | t0002 | g0101 | AFR | LWK | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19055 | hp2 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19057 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19058 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19063 | hp2 | a0001 | c0002 | t0002 | g0072 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19068 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19074 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19077 | hp2 | a0001 | c0002 | t0002 | g0088 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19078 | hp1 | a0001 | c0002 | t0002 | g0081 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19078 | hp2 | a0001 | c0001 | t0006 | g0026 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19082 | hp2 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19083 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19084 | hp1 | a0006 | c0011 | t0002 | g0039 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19088 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19089 | hp2 | a0001 | c0002 | t0002 | g0063 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19240 | hp1 | a0004 | c0006 | t0001 | g0024 | AFR | YRI | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA19240 | hp2 | a0018 | c0024 | t0001 | g0196 | AFR | YRI | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | ASW | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA20129 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | ASW | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | TSI | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0015 | EUR | TSI | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0222 | EUR | TSI | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA20805 | hp2 | a0001 | c0002 | t0001 | g0083 | EUR | TSI | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0186 | SAS | GIH | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA20905 | hp2 | a0003 | c0004 | t0001 | g0002 | SAS | GIH | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02109 | hp1 | a0002 | c0003 | t0002 | g0008 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02109 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0009 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02486 | hp2 | a0002 | c0003 | t0002 | g0109 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02559 | hp1 | a0001 | c0025 | t0001 | g0130 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03471 | hp1 | a0017 | c0027 | t0002 | g0225 | AFR | MSL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | MSL | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG06807 | hp1 | a0002 | c0003 | t0002 | g0008 | AFR | USA | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
HG06807 | hp2 | a0002 | c0003 | t0002 | g0128 | AFR | USA | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | LWK | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
NA21309 | hp2 | a0002 | c0003 | t0001 | g0097 | AFR | LWK | MAN1B1_chr9_137081985_137114183 | MAN1B1 | chr9 | 137081985 | 137114183 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:137087175 | A | G | 16 | a0001 a0003 a0004 others(13): Show |
368 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(365): Show |
missense_variant | MODERATE | c.176A>G | p.Asn59Ser | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 1/13 | 191/2707 | 176/2100 | 59/699 | chr9 | 137087175 | |||
chr9:137088878 | T | C | 1 | a0009 | 1 | HG00558.hp2 | missense_variant | MODERATE | c.338T>C | p.Phe113Ser | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/13 | 353/2707 | 338/2100 | 113/699 | chr9 | 137088878 | |||
chr9:137088887 | A | G | 3 | a0006 a0016 a0017 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
missense_variant | MODERATE | c.347A>G | p.Glu116Gly | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/13 | 362/2707 | 347/2100 | 116/699 | chr9 | 137088887 | |||
chr9:137088943 | G | A | 1 | a0014 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.403G>A | p.Val135Ile | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/13 | 418/2707 | 403/2100 | 135/699 | chr9 | 137088943 | |||
chr9:137096361 | C | T | 1 | a0003 | 9 | HG01109.hp2 HG01257.hp1 HG01258.hp2 others(6): Show |
missense_variant | MODERATE | c.590C>T | p.Pro197Leu | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/13 | 605/2707 | 590/2100 | 197/699 | chr9 | 137096361 | |||
chr9:137096373 | C | T | 2 | a0004 a0015 |
5 | HG02717.hp1 HG02886.hp2 HG02896.hp2 others(2): Show |
missense_variant | MODERATE | c.602C>T | p.Pro201Leu | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/13 | 617/2707 | 602/2100 | 201/699 | chr9 | 137096373 | |||
chr9:137097842 | T | G | 1 | a0008 | 1 | HG00140.hp2 | missense_variant | MODERATE | c.635T>G | p.Val212Gly | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/13 | 650/2707 | 635/2100 | 212/699 | chr9 | 137097842 | |||
chr9:137097914 | C | T | 1 | a0016 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.707C>T | p.Pro236Leu | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/13 | 722/2707 | 707/2100 | 236/699 | chr9 | 137097914 | |||
chr9:137099759 | G | A | 1 | a0015 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.794G>A | p.Arg265His | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 6/13 | 809/2707 | 794/2100 | 265/699 | chr9 | 137099759 | |||
chr9:137101647 | G | A | 1 | a0010 | 1 | HG00673.hp2 | missense_variant | MODERATE | c.1229G>A | p.Arg410His | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/13 | 1244/2707 | 1229/2100 | 410/699 | chr9 | 137101647 | |||
chr9:137106299 | G | A | 1 | a0005 | 3 | HG02630.hp1 HG03516.hp2 NA19043.hp2 |
missense_variant | MODERATE | c.1429G>A | p.Gly477Arg | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 9/13 | 1444/2707 | 1429/2100 | 477/699 | chr9 | 137106299 | |||
chr9:137106742 | G | A | 1 | a0006 | 2 | NA18978.hp2 NA19084.hp1 |
missense_variant | MODERATE | c.1499G>A | p.Arg500Gln | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 10/13 | 1514/2707 | 1499/2100 | 500/699 | chr9 | 137106742 | |||
chr9:137106745 | A | G | 1 | a0007 | 2 | NA18980.hp2 NA18984.hp1 |
missense_variant | MODERATE | c.1502A>G | p.His501Arg | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 10/13 | 1517/2707 | 1502/2100 | 501/699 | chr9 | 137106745 | |||
chr9:137107419 | A | G | 1 | a0018 | 1 | NA19240.hp2 | missense_variant | MODERATE | c.1736A>G | p.Gln579Arg | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 11/13 | 1751/2707 | 1736/2100 | 579/699 | chr9 | 137107419 | |||
chr9:137107428 | G | A | 1 | a0013 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.1745G>A | p.Arg582His | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 11/13 | 1760/2707 | 1745/2100 | 582/699 | chr9 | 137107428 | |||
chr9:137108482 | C | T | 1 | a0011 | 1 | HG01943.hp1 | missense_variant | MODERATE | c.1991C>T | p.Thr664Met | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 13/13 | 2006/2707 | 1991/2100 | 664/699 | chr9 | 137108482 | |||
chr9:137108511 | G | A | 1 | a0012 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.2020G>A | p.Asp674Asn | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 13/13 | 2035/2707 | 2020/2100 | 674/699 | chr9 | 137108511 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:137087035 | C | G | 1 | a0001c0029 | 1 | HG02698.hp2 | synonymous_variant | LOW | c.36C>G | p.Leu12Leu | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 1/13 | 51/2707 | 36/2100 | 12/699 | chr9 | 137087035 | |||
chr9:137087182 | C | T | 1 | a0001c0007 | 3 | HG01074.hp1 HG02647.hp2 HG02976.hp2 |
synonymous_variant | LOW | c.183C>T | p.Asp61Asp | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 1/13 | 198/2707 | 183/2100 | 61/699 | chr9 | 137087182 | |||
chr9:137088999 | G | A | 1 | a0002c0012 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.459G>A | p.Ser153Ser | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/13 | 474/2707 | 459/2100 | 153/699 | chr9 | 137088999 | |||
chr9:137097915 | G | A | 1 | a0015c0026 | 1 | HG02896.hp2 | synonymous_variant | LOW | c.708G>A | p.Pro236Pro | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/13 | 723/2707 | 708/2100 | 236/699 | chr9 | 137097915 | |||
chr9:137099709 | T | C | 1 | a0006c0011 | 2 | NA18978.hp2 NA19084.hp1 |
synonymous_variant | LOW | c.744T>C | p.Tyr248Tyr | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 6/13 | 759/2707 | 744/2100 | 248/699 | chr9 | 137099709 | |||
chr9:137099826 | C | T | 1 | a0006c0011 | 2 | NA18978.hp2 NA19084.hp1 |
synonymous_variant | LOW | c.861C>T | p.Leu287Leu | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 6/13 | 876/2707 | 861/2100 | 287/699 | chr9 | 137099826 | |||
chr9:137101513 | C | T | 1 | a0016c0028 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.1095C>T | p.Ala365Ala | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/13 | 1110/2707 | 1095/2100 | 365/699 | chr9 | 137101513 | |||
chr9:137101543 | G | A | 1 | a0001c0017 | 1 | NA18942.hp1 | synonymous_variant | LOW | c.1125G>A | p.Ser375Ser | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/13 | 1140/2707 | 1125/2100 | 375/699 | chr9 | 137101543 | |||
chr9:137101564 | A | G | 2 | a0001c0025 a0002c0009 |
3 | HG01891.hp1 HG02280.hp2 HG02559.hp1 |
synonymous_variant | LOW | c.1146A>G | p.Gly382Gly | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/13 | 1161/2707 | 1146/2100 | 382/699 | chr9 | 137101564 | |||
chr9:137106256 | C | T | 1 | a0016c0028 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.1386C>T | p.Ala462Ala | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 9/13 | 1401/2707 | 1386/2100 | 462/699 | chr9 | 137106256 | |||
chr9:137106728 | A | G | 2 | a0006c0011 a0016c0028 |
3 | HG03225.hp2 NA18978.hp2 NA19084.hp1 |
synonymous_variant | LOW | c.1485A>G | p.Arg495Arg | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 10/13 | 1500/2707 | 1485/2100 | 495/699 | chr9 | 137106728 | |||
chr9:137107393 | G | A | 1 | a0016c0028 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.1710G>A | p.Glu570Glu | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 11/13 | 1725/2707 | 1710/2100 | 570/699 | chr9 | 137107393 | |||
chr9:137107396 | C | T | 1 | a0005c0008 | 2 | HG03516.hp2 NA19043.hp2 |
synonymous_variant | LOW | c.1713C>T | p.Ile571Ile | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 11/13 | 1728/2707 | 1713/2100 | 571/699 | chr9 | 137107396 | |||
chr9:137107444 | C | G | 1 | a0017c0027 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.1761C>G | p.Val587Val | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 11/13 | 1776/2707 | 1761/2100 | 587/699 | chr9 | 137107444 | |||
chr9:137107566 | C | T | 1 | a0001c0023 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.1800C>T | p.Thr600Thr | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 12/13 | 1815/2707 | 1800/2100 | 600/699 | chr9 | 137107566 | |||
chr9:137107611 | A | G | 1 | a0017c0027 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.1845A>G | p.Lys615Lys | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 12/13 | 1860/2707 | 1845/2100 | 615/699 | chr9 | 137107611 | |||
chr9:137108396 | G | T | 1 | a0017c0027 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.1905G>T | p.Ser635Ser | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 13/13 | 1920/2707 | 1905/2100 | 635/699 | chr9 | 137108396 | |||
chr9:137108423 | C | T | 1 | a0001c0022 | 1 | HG01258.hp1 | synonymous_variant | LOW | c.1932C>T | p.Val644Val | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 13/13 | 1947/2707 | 1932/2100 | 644/699 | chr9 | 137108423 | |||
chr9:137108447 | T | C | 1 | a0017c0027 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.1956T>C | p.Pro652Pro | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 13/13 | 1971/2707 | 1956/2100 | 652/699 | chr9 | 137108447 | |||
chr9:137108537 | T | C | 24 | a0001c0001 a0001c0005 a0001c0007 others(21): Show |
321 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(318): Show |
synonymous_variant | LOW | c.2046T>C | p.Asp682Asp | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 13/13 | 2061/2707 | 2046/2100 | 682/699 | chr9 | 137108537 | |||
chr9:137108543 | C | T | 1 | a0001c0005 | 6 | HG00642.hp2 HG01074.hp2 HG01167.hp2 others(3): Show |
synonymous_variant | LOW | c.2052C>T | p.Tyr684Tyr | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 13/13 | 2067/2707 | 2052/2100 | 684/699 | chr9 | 137108543 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:137108748 | C | G | 1 | a0001c0001t0005 | 6 | HG02109.hp2 HG02809.hp2 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*157C>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 13/13 | 157 | chr9 | 137108748 | ||||||
chr9:137108776 | T | G | 1 | a0001c0001t0006 | 4 | NA18969.hp1 NA18981.hp1 NA18997.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*185T>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 13/13 | 185 | chr9 | 137108776 | ||||||
chr9:137108975 | A | G | 18 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(15): Show |
240 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(237): Show |
3_prime_UTR_variant | MODIFIER | c.*384A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 13/13 | 384 | chr9 | 137108975 | ||||||
chr9:137109070 | C | T | 1 | a0001c0001t0007 | 2 | HG03041.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*479C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 13/13 | 479 | chr9 | 137109070 | ||||||
chr9:137109077 | G | GC | 3 | a0001c0001t0003 a0001c0002t0004 a0001c0005t0004 |
27 | HG00280.hp1 HG00558.hp1 HG00642.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*488dupC | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 13/13 | 489 | INFO_REALIGN_3_PRIME | chr9 | 137109077 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr9:137087266 | C | T | 1 | a0017c0027t0002g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.219+48C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 1/12 | chr9 | 137087266 | |||||||
chr9:137087344 | C | A | 1 | a0001c0001t0001g0050 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.219+126C>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 1/12 | chr9 | 137087344 | |||||||
chr9:137087595 | T | G | 2 | a0001c0001t0001g0027 a0001c0001t0003g0027 |
2 | HG02602.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.219+377T>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 1/12 | chr9 | 137087595 | |||||||
chr9:137087601 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.219+383C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 1/12 | chr9 | 137087601 | |||||||
chr9:137087753 | C | T | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG03834.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.220-322C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 1/12 | chr9 | 137087753 | |||||||
chr9:137088055 | A | C | 1 | a0017c0027t0002g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.220-20A>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 1/12 | chr9 | 137088055 | |||||||
chr9:137088239 | G | A | 1 | a0002c0003t0002g0019 | 3 | HG02572.hp1 HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.328+56G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 2/12 | chr9 | 137088239 | |||||||
chr9:137088416 | C | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(124): Show |
221 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.328+233C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 2/12 | chr9 | 137088416 | |||||||
chr9:137088420 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.328+237C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 2/12 | chr9 | 137088420 | |||||||
chr9:137088572 | T | C | 1 | a0001c0002t0002g0051 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.329-297T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 2/12 | chr9 | 137088572 | |||||||
chr9:137088678 | G | T | 1 | a0001c0025t0001g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.329-191G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 2/12 | chr9 | 137088678 | |||||||
chr9:137089028 | G | T | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+23G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137089028 | |||||||
chr9:137089066 | A | G | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+61A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137089066 | |||||||
chr9:137089067 | C | T | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+62C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137089067 | |||||||
chr9:137089174 | T | C | 1 | a0001c0001t0002g0052 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.465+169T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137089174 | |||||||
chr9:137089175 | T | C | 6 | a0001c0001t0002g0028 a0001c0001t0002g0053 a0001c0001t0002g0054 others(3): Show |
7 | HG00323.hp2 HG01168.hp1 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.465+170T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137089175 | |||||||
chr9:137089187 | T | C | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+182T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137089187 | |||||||
chr9:137089241 | A | G | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+236A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137089241 | |||||||
chr9:137089324 | A | G | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+319A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137089324 | |||||||
chr9:137089385 | G | A | 1 | a0001c0001t0001g0022 | 3 | NA19004.hp1 NA19060.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.465+380G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137089385 | |||||||
chr9:137089626 | A | G | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
319 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.465+621A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137089626 | |||||||
chr9:137089751 | G | A | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+746G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137089751 | |||||||
chr9:137089767 | C | T | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.465+762C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137089767 | |||||||
chr9:137089796 | T | C | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+791T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137089796 | |||||||
chr9:137089851 | C | T | 9 | a0001c0001t0001g0014 a0001c0001t0001g0050 a0001c0001t0001g0216 others(6): Show |
14 | HG01106.hp1 HG01123.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.465+846C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137089851 | |||||||
chr9:137089929 | C | G | 1 | a0001c0007t0001g0215 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.465+924C>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137089929 | |||||||
chr9:137090171 | G | A | 23 | a0002c0003t0001g0021 a0002c0003t0001g0094 a0002c0003t0001g0095 others(20): Show |
35 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.465+1166G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137090171 | |||||||
chr9:137090241 | G | A | 1 | a0001c0001t0001g0132 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.465+1236G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137090241 | |||||||
chr9:137090275 | G | T | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.465+1270G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137090275 | |||||||
chr9:137090411 | G | A | 1 | a0010c0018t0002g0058 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.465+1406G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137090411 | |||||||
chr9:137090459 | G | A | 2 | a0006c0011t0002g0039 a0016c0028t0002g0129 |
3 | HG03225.hp2 NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.465+1454G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137090459 | |||||||
chr9:137090558 | G | C | 1 | a0001c0025t0001g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.465+1553G>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137090558 | |||||||
chr9:137090633 | G | A | 23 | a0002c0003t0001g0021 a0002c0003t0001g0094 a0002c0003t0001g0095 others(20): Show |
35 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.465+1628G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137090633 | |||||||
chr9:137090664 | C | T | 2 | a0006c0011t0002g0039 a0016c0028t0002g0129 |
3 | HG03225.hp2 NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.465+1659C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137090664 | |||||||
chr9:137090697 | G | A | 2 | a0002c0003t0002g0091 a0002c0003t0002g0128 |
2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.465+1692G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137090697 | |||||||
chr9:137090707 | C | T | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
319 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.465+1702C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137090707 | |||||||
chr9:137090724 | G | T | 1 | a0001c0002t0002g0090 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.465+1719G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137090724 | |||||||
chr9:137090965 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.465+1960C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137090965 | |||||||
chr9:137090966 | G | A | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.465+1961G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137090966 | |||||||
chr9:137090984 | G | C | 1 | a0001c0002t0004g0059 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.465+1979G>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137090984 | |||||||
chr9:137090996 | C | T | 5 | a0001c0001t0001g0213 a0001c0002t0002g0089 a0001c0007t0001g0211 others(2): Show |
5 | HG01074.hp1 HG01928.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.465+1991C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137090996 | |||||||
chr9:137091038 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.465+2033C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137091038 | |||||||
chr9:137091358 | G | A | 24 | a0002c0003t0001g0021 a0002c0003t0001g0094 a0002c0003t0001g0095 others(21): Show |
36 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.465+2353G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137091358 | |||||||
chr9:137091521 | A | AT | 32 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(29): Show |
41 | HG00323.hp2 HG00642.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.465+2539dupT | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr9 | 137091521 | ||||||
chr9:137091521 | A | ATT | 8 | a0001c0001t0001g0037 a0001c0001t0002g0038 a0001c0001t0002g0052 others(5): Show |
10 | HG00140.hp1 HG00140.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.465+2538_465+2539d others(4): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr9 | 137091521 | ||||||
chr9:137091521 | A | T | 25 | a0001c0002t0002g0031 a0002c0003t0001g0021 a0002c0003t0001g0094 others(22): Show |
38 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.465+2516A>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137091521 | |||||||
chr9:137091521 | AT | A | 116 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(113): Show |
204 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(201): Show |
intron_variant | MODIFIER | c.465+2539delT | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr9 | 137091521 | ||||||
chr9:137091521 | ATT | A | 6 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0139 others(3): Show |
6 | HG01943.hp2 HG02976.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.465+2538_465+2539d others(4): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr9 | 137091521 | ||||||
chr9:137091524 | T | A | 3 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 |
3 | HG00438.hp1 HG00597.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.465+2519T>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137091524 | |||||||
chr9:137091528 | T | A | 23 | a0002c0003t0001g0021 a0002c0003t0001g0094 a0002c0003t0001g0095 others(20): Show |
35 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.465+2523T>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137091528 | |||||||
chr9:137091532 | T | A | 12 | a0002c0003t0001g0021 a0002c0003t0001g0094 a0002c0003t0001g0095 others(9): Show |
16 | HG01884.hp1 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.465+2527T>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137091532 | |||||||
chr9:137091545 | G | T | 1 | a0001c0025t0001g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.465+2540G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137091545 | |||||||
chr9:137091565 | T | C | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+2560T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137091565 | |||||||
chr9:137091576 | C | T | 2 | a0006c0011t0002g0039 a0016c0028t0002g0129 |
3 | HG03225.hp2 NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.465+2571C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137091576 | |||||||
chr9:137091641 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.465+2636C>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137091641 | |||||||
chr9:137091676 | G | A | 1 | a0017c0027t0002g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.465+2671G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137091676 | |||||||
chr9:137091715 | A | G | 1 | a0001c0002t0002g0085 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.465+2710A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137091715 | |||||||
chr9:137091761 | C | T | 24 | a0002c0003t0001g0021 a0002c0003t0001g0094 a0002c0003t0001g0095 others(21): Show |
36 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(33): Show |
intron_variant | MODIFIER | c.465+2756C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137091761 | |||||||
chr9:137092190 | C | G | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+3185C>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137092190 | |||||||
chr9:137092199 | C | CA | 26 | a0001c0001t0001g0141 a0001c0001t0003g0140 a0001c0002t0001g0064 others(23): Show |
38 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.465+3208dupA | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr9 | 137092199 | ||||||
chr9:137092217 | G | T | 1 | a0001c0001t0001g0202 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.465+3212G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137092217 | |||||||
chr9:137092321 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.465+3316A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137092321 | |||||||
chr9:137092388 | C | CATTGAGG others(43): Show |
3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.465+3409_465+3458d others(52): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr9 | 137092388 | ||||||
chr9:137092395 | G | C | 1 | a0003c0004t0001g0142 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.465+3390G>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137092395 | |||||||
chr9:137092882 | C | T | 2 | a0001c0001t0005g0012 a0001c0001t0005g0113 |
6 | HG02109.hp2 HG02809.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.466-3355C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137092882 | |||||||
chr9:137092898 | C | T | 36 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(33): Show |
47 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(44): Show |
intron_variant | MODIFIER | c.466-3339C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137092898 | |||||||
chr9:137093091 | T | C | 1 | a0016c0028t0002g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.466-3146T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137093091 | |||||||
chr9:137093111 | T | A | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-3126T>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137093111 | |||||||
chr9:137093125 | A | G | 25 | a0001c0001t0002g0123 a0002c0003t0001g0021 a0002c0003t0001g0094 others(22): Show |
37 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(34): Show |
intron_variant | MODIFIER | c.466-3112A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137093125 | |||||||
chr9:137093237 | T | C | 1 | a0001c0002t0002g0065 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.466-3000T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137093237 | |||||||
chr9:137093304 | A | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(96): Show |
179 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.466-2933A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137093304 | |||||||
chr9:137093362 | A | G | 1 | a0005c0008t0002g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.466-2875A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137093362 | |||||||
chr9:137093440 | T | C | 2 | a0001c0001t0002g0123 a0002c0003t0002g0128 |
2 | HG06807.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.466-2797T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137093440 | |||||||
chr9:137093514 | C | A | 1 | a0001c0001t0002g0124 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.466-2723C>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137093514 | |||||||
chr9:137093693 | G | A | 1 | a0001c0001t0003g0143 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.466-2544G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137093693 | |||||||
chr9:137093695 | G | A | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-2542G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137093695 | |||||||
chr9:137093748 | G | A | 1 | a0002c0003t0002g0092 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.466-2489G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137093748 | |||||||
chr9:137093750 | C | T | 1 | a0001c0001t0001g0200 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.466-2487C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137093750 | |||||||
chr9:137093813 | G | A | 1 | a0001c0001t0002g0222 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.466-2424G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137093813 | |||||||
chr9:137093827 | C | CT | 1 | a0004c0006t0001g0024 | 3 | HG02886.hp2 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.466-2409dupT | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr9 | 137093827 | ||||||
chr9:137093875 | G | T | 1 | a0001c0001t0001g0199 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.466-2362G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137093875 | |||||||
chr9:137094013 | T | C | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-2224T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137094013 | |||||||
chr9:137094014 | G | A | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-2223G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137094014 | |||||||
chr9:137094018 | A | AT | 32 | a0001c0001t0001g0135 a0001c0001t0001g0197 a0001c0001t0001g0198 others(29): Show |
50 | HG00099.hp2 HG00609.hp2 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.466-2205dupT | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr9 | 137094018 | ||||||
chr9:137094079 | A | G | 1 | a0001c0001t0001g0047 | 2 | HG00099.hp1 HG01168.hp2 |
intron_variant | MODIFIER | c.466-2158A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137094079 | |||||||
chr9:137094103 | G | A | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-2134G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137094103 | |||||||
chr9:137094302 | A | C | 1 | a0001c0001t0001g0017 | 4 | HG00280.hp2 HG00323.hp1 HG02683.hp1 others(1): Show |
intron_variant | MODIFIER | c.466-1935A>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137094302 | |||||||
chr9:137094322 | C | T | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-1915C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137094322 | |||||||
chr9:137094375 | C | T | 1 | a0016c0028t0002g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.466-1862C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137094375 | |||||||
chr9:137094402 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.466-1835G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137094402 | |||||||
chr9:137094557 | T | C | 1 | a0016c0028t0002g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.466-1680T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137094557 | |||||||
chr9:137094565 | C | A | 1 | a0005c0008t0002g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.466-1672C>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137094565 | |||||||
chr9:137094577 | T | TA | 6 | a0001c0001t0001g0197 a0001c0001t0001g0204 a0001c0002t0002g0006 others(3): Show |
13 | HG00621.hp2 HG02040.hp2 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.466-1649dupA | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr9 | 137094577 | ||||||
chr9:137094708 | G | C | 1 | a0001c0001t0001g0158 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.466-1529G>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137094708 | |||||||
chr9:137094748 | C | T | 1 | a0016c0028t0002g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.466-1489C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137094748 | |||||||
chr9:137094773 | A | G | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-1464A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137094773 | |||||||
chr9:137094895 | C | CA | 5 | a0001c0001t0002g0053 a0001c0002t0002g0066 a0001c0002t0002g0069 others(2): Show |
5 | HG01496.hp1 HG02056.hp1 HG03710.hp1 others(2): Show |
intron_variant | MODIFIER | c.466-1334dupA | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr9 | 137094895 | ||||||
chr9:137094920 | G | A | 1 | a0001c0002t0001g0070 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.466-1317G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137094920 | |||||||
chr9:137094930 | G | A | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-1307G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137094930 | |||||||
chr9:137095044 | C | T | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-1193C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095044 | |||||||
chr9:137095094 | A | G | 1 | a0001c0002t0002g0068 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.466-1143A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095094 | |||||||
chr9:137095095 | G | A | 1 | a0001c0002t0002g0068 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.466-1142G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095095 | |||||||
chr9:137095173 | A | G | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-1064A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095173 | |||||||
chr9:137095199 | G | A | 3 | a0001c0002t0002g0009 a0001c0002t0002g0069 a0001c0002t0002g0086 |
8 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.466-1038G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095199 | |||||||
chr9:137095203 | G | A | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-1034G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095203 | |||||||
chr9:137095227 | G | A | 1 | a0001c0001t0002g0110 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.466-1010G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095227 | |||||||
chr9:137095327 | A | G | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-910A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095327 | |||||||
chr9:137095367 | C | T | 1 | a0001c0002t0002g0068 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.466-870C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095367 | |||||||
chr9:137095368 | T | C | 1 | a0001c0002t0002g0068 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.466-869T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095368 | |||||||
chr9:137095373 | T | A | 1 | a0001c0002t0002g0071 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.466-864T>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095373 | |||||||
chr9:137095373 | TA | T | 11 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(8): Show |
11 | HG01074.hp1 HG01074.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.466-851delA | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr9 | 137095373 | ||||||
chr9:137095374 | A | T | 48 | a0001c0001t0001g0002 a0001c0001t0001g0032 a0001c0001t0001g0033 others(45): Show |
69 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.466-863A>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095374 | |||||||
chr9:137095375 | A | T | 3 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0007t0001g0212 |
3 | HG01074.hp1 HG01496.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.466-862A>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095375 | |||||||
chr9:137095389 | G | A | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-848G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095389 | |||||||
chr9:137095392 | G | A | 26 | a0001c0001t0002g0123 a0002c0003t0001g0021 a0002c0003t0001g0094 others(23): Show |
39 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(36): Show |
intron_variant | MODIFIER | c.466-845G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095392 | |||||||
chr9:137095433 | C | T | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-804C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095433 | |||||||
chr9:137095541 | A | C | 2 | a0006c0011t0002g0039 a0016c0028t0002g0129 |
3 | HG03225.hp2 NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.466-696A>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095541 | |||||||
chr9:137095609 | C | A | 2 | a0001c0001t0001g0032 a0001c0001t0002g0032 |
2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.466-628C>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095609 | |||||||
chr9:137095759 | A | G | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-478A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095759 | |||||||
chr9:137095772 | C | G | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.466-465C>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095772 | |||||||
chr9:137095840 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0131 |
3 | NA18963.hp1 NA18987.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.466-397G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095840 | |||||||
chr9:137095901 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.466-336G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095901 | |||||||
chr9:137095906 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.466-331G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095906 | |||||||
chr9:137095922 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0193 |
2 | HG02523.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.466-315G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137095922 | |||||||
chr9:137096078 | T | C | 69 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(66): Show |
128 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.466-159T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137096078 | |||||||
chr9:137096094 | G | A | 23 | a0002c0003t0001g0021 a0002c0003t0001g0094 a0002c0003t0001g0095 others(20): Show |
35 | HG01243.hp2 HG01884.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.466-143G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137096094 | |||||||
chr9:137096105 | C | T | 2 | a0002c0003t0002g0092 a0002c0003t0002g0100 |
2 | HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.466-132C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137096105 | |||||||
chr9:137096221 | A | G | 1 | a0001c0002t0002g0067 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.466-16A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 3/12 | chr9 | 137096221 | |||||||
chr9:137096405 | G | A | 1 | a0001c0002t0002g0072 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.620+14G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137096405 | |||||||
chr9:137096417 | G | A | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+26G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137096417 | |||||||
chr9:137096434 | G | T | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+43G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137096434 | |||||||
chr9:137096454 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(194): Show |
319 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.620+63T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137096454 | |||||||
chr9:137096648 | A | G | 1 | a0005c0008t0002g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.620+257A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137096648 | |||||||
chr9:137096654 | G | A | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+263G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137096654 | |||||||
chr9:137096742 | A | G | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+351A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137096742 | |||||||
chr9:137096755 | G | A | 1 | a0006c0011t0002g0039 | 2 | NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.620+364G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137096755 | |||||||
chr9:137096776 | C | A | 1 | a0001c0002t0002g0068 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.620+385C>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137096776 | |||||||
chr9:137096905 | G | A | 1 | a0005c0008t0002g0101 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.620+514G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137096905 | |||||||
chr9:137096911 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.620+520G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137096911 | |||||||
chr9:137096932 | C | T | 2 | a0001c0001t0006g0026 a0001c0001t0006g0180 |
4 | NA18969.hp1 NA18981.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.620+541C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137096932 | |||||||
chr9:137097034 | C | T | 1 | a0017c0027t0002g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.620+643C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137097034 | |||||||
chr9:137097070 | G | A | 1 | a0017c0027t0002g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.620+679G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137097070 | |||||||
chr9:137097186 | G | A | 1 | a0001c0001t0002g0052 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.621-642G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137097186 | |||||||
chr9:137097195 | G | A | 1 | a0006c0011t0002g0039 | 2 | NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.621-633G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137097195 | |||||||
chr9:137097343 | C | G | 2 | a0006c0011t0002g0039 a0017c0027t0002g0225 |
3 | HG03471.hp1 NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.621-485C>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137097343 | |||||||
chr9:137097389 | T | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0027 others(30): Show |
50 | HG00280.hp1 HG00558.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.621-439T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137097389 | |||||||
chr9:137097429 | C | T | 3 | a0001c0007t0001g0211 a0001c0007t0001g0212 a0001c0007t0001g0215 |
3 | HG01074.hp1 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.621-399C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137097429 | |||||||
chr9:137097430 | G | A | 1 | a0006c0011t0002g0039 | 2 | NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.621-398G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137097430 | |||||||
chr9:137097437 | G | A | 11 | a0001c0001t0001g0218 a0002c0003t0001g0021 a0002c0003t0001g0094 others(8): Show |
15 | HG01361.hp2 HG01884.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.621-391G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137097437 | |||||||
chr9:137097526 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.621-302C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137097526 | |||||||
chr9:137097654 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0001g0181 |
2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.621-174G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137097654 | |||||||
chr9:137097789 | T | C | 1 | a0001c0023t0001g0182 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.621-39T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 4/12 | chr9 | 137097789 | |||||||
chr9:137097965 | C | T | 1 | a0002c0003t0002g0107 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.730+28C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137097965 | |||||||
chr9:137097971 | C | T | 1 | a0001c0001t0002g0036 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.730+34C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137097971 | |||||||
chr9:137098026 | C | T | 1 | a0016c0028t0002g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.730+89C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137098026 | |||||||
chr9:137098027 | G | C | 64 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0018 others(61): Show |
118 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.730+90G>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137098027 | |||||||
chr9:137098140 | A | G | 2 | a0002c0009t0002g0104 a0002c0009t0002g0105 |
2 | HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.730+203A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137098140 | |||||||
chr9:137098237 | C | T | 1 | a0001c0002t0001g0070 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.730+300C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137098237 | |||||||
chr9:137098287 | G | A | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.730+350G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137098287 | |||||||
chr9:137098292 | T | C | 41 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(38): Show |
54 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(51): Show |
intron_variant | MODIFIER | c.730+355T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137098292 | |||||||
chr9:137098310 | C | T | 4 | a0002c0003t0002g0008 a0002c0003t0002g0106 a0002c0003t0002g0107 others(1): Show |
10 | HG01243.hp2 HG02109.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.730+373C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137098310 | |||||||
chr9:137098366 | C | T | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.730+429C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137098366 | |||||||
chr9:137098455 | G | T | 122 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(119): Show |
215 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.730+518G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137098455 | |||||||
chr9:137098559 | G | A | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.730+622G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137098559 | |||||||
chr9:137098696 | C | T | 1 | a0002c0003t0002g0099 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.730+759C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137098696 | |||||||
chr9:137098703 | A | G | 1 | a0001c0002t0002g0072 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.730+766A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137098703 | |||||||
chr9:137098723 | T | C | 1 | a0001c0002t0002g0074 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.730+786T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137098723 | |||||||
chr9:137098732 | G | A | 3 | a0001c0001t0001g0045 a0001c0001t0001g0139 a0001c0001t0001g0185 |
4 | HG00738.hp2 HG01261.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.730+795G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137098732 | |||||||
chr9:137098771 | T | G | 1 | a0001c0001t0003g0049 | 2 | HG01496.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.730+834T>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137098771 | |||||||
chr9:137098842 | C | A | 1 | a0001c0001t0007g0154 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.731-854C>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137098842 | |||||||
chr9:137098853 | G | A | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.731-843G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137098853 | |||||||
chr9:137098858 | T | A | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.731-838T>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137098858 | |||||||
chr9:137098970 | T | C | 2 | a0002c0009t0002g0104 a0002c0009t0002g0105 |
2 | HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.731-726T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137098970 | |||||||
chr9:137099038 | G | C | 1 | a0001c0002t0002g0075 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.731-658G>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137099038 | |||||||
chr9:137099083 | G | T | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.731-613G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137099083 | |||||||
chr9:137099084 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(129): Show |
229 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.731-612C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137099084 | |||||||
chr9:137099087 | C | A | 6 | a0002c0003t0002g0020 a0002c0003t0002g0092 a0002c0003t0002g0100 others(3): Show |
8 | HG02630.hp1 HG02965.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.731-609C>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137099087 | |||||||
chr9:137099140 | A | C | 18 | a0001c0001t0002g0110 a0002c0003t0002g0008 a0002c0003t0002g0019 others(15): Show |
28 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.731-556A>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137099140 | |||||||
chr9:137099167 | G | A | 24 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0027 others(21): Show |
37 | HG00280.hp1 HG00558.hp1 HG01070.hp1 others(34): Show |
intron_variant | MODIFIER | c.731-529G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137099167 | |||||||
chr9:137099169 | G | A | 1 | a0001c0001t0003g0144 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.731-527G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137099169 | |||||||
chr9:137099236 | G | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0170 a0001c0001t0001g0171 others(2): Show |
10 | NA18944.hp1 NA18947.hp2 NA18965.hp2 others(7): Show |
intron_variant | MODIFIER | c.731-460G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137099236 | |||||||
chr9:137099262 | G | A | 1 | a0017c0027t0002g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.731-434G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137099262 | |||||||
chr9:137099266 | G | A | 2 | a0001c0001t0001g0037 a0001c0001t0001g0131 |
3 | NA18963.hp1 NA18987.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.731-430G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137099266 | |||||||
chr9:137099303 | G | A | 17 | a0002c0003t0002g0008 a0002c0003t0002g0019 a0002c0003t0002g0020 others(14): Show |
27 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.731-393G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137099303 | |||||||
chr9:137099403 | G | C | 1 | a0001c0001t0001g0029 | 2 | HG00741.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.731-293G>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137099403 | |||||||
chr9:137099443 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.731-253G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137099443 | |||||||
chr9:137099456 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.731-240G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137099456 | |||||||
chr9:137099571 | G | A | 6 | a0002c0003t0002g0020 a0002c0003t0002g0092 a0002c0003t0002g0100 others(3): Show |
8 | HG02630.hp1 HG02965.hp2 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.731-125G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137099571 | |||||||
chr9:137099647 | G | A | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG03834.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.731-49G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137099647 | |||||||
chr9:137099650 | G | A | 185 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(182): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.731-46G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 5/12 | chr9 | 137099650 | |||||||
chr9:137099959 | G | A | 2 | a0001c0001t0001g0185 a0001c0023t0001g0182 |
2 | HG00738.hp2 HG01192.hp1 |
intron_variant | MODIFIER | c.916+78G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 6/12 | chr9 | 137099959 | |||||||
chr9:137100127 | C | T | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.916+246C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 6/12 | chr9 | 137100127 | |||||||
chr9:137100162 | C | G | 1 | a0006c0011t0002g0039 | 2 | NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.916+281C>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 6/12 | chr9 | 137100162 | |||||||
chr9:137100265 | T | C | 1 | a0001c0001t0001g0184 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.916+384T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 6/12 | chr9 | 137100265 | |||||||
chr9:137100372 | G | A | 1 | a0016c0028t0002g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.916+491G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 6/12 | chr9 | 137100372 | |||||||
chr9:137100411 | C | T | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.916+530C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 6/12 | chr9 | 137100411 | |||||||
chr9:137100429 | TGAC | T | 2 | a0006c0011t0002g0039 a0016c0028t0002g0129 |
3 | HG03225.hp2 NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.916+552_916+554del others(3): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137100429 | ||||||
chr9:137100453 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.917-552T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 6/12 | chr9 | 137100453 | |||||||
chr9:137100495 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(129): Show |
229 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.917-510C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 6/12 | chr9 | 137100495 | |||||||
chr9:137100571 | G | A | 1 | a0001c0001t0001g0219 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.917-434G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 6/12 | chr9 | 137100571 | |||||||
chr9:137100613 | C | A | 36 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(33): Show |
46 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.917-392C>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 6/12 | chr9 | 137100613 | |||||||
chr9:137100683 | G | C | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.917-322G>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 6/12 | chr9 | 137100683 | |||||||
chr9:137100776 | T | C | 58 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(55): Show |
79 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.917-229T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 6/12 | chr9 | 137100776 | |||||||
chr9:137100839 | C | G | 2 | a0001c0001t0001g0023 a0001c0001t0001g0141 |
4 | NA18945.hp2 NA18953.hp1 NA19011.hp1 others(1): Show |
intron_variant | MODIFIER | c.917-166C>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 6/12 | chr9 | 137100839 | |||||||
chr9:137100909 | C | CA | 36 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(33): Show |
46 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.917-95dupA | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr9 | 137100909 | ||||||
chr9:137100939 | A | C | 1 | a0001c0001t0002g0110 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.917-66A>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 6/12 | chr9 | 137100939 | |||||||
chr9:137101169 | T | A | 1 | a0001c0001t0003g0146 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1065+16T>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 7/12 | chr9 | 137101169 | |||||||
chr9:137101265 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1065+112C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 7/12 | chr9 | 137101265 | |||||||
chr9:137101361 | C | G | 3 | a0001c0007t0001g0211 a0001c0007t0001g0212 a0001c0007t0001g0215 |
3 | HG01074.hp1 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1066-123C>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 7/12 | chr9 | 137101361 | |||||||
chr9:137101417 | A | G | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1066-67A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 7/12 | chr9 | 137101417 | |||||||
chr9:137101455 | G | A | 1 | a0017c0027t0002g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1066-29G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 7/12 | chr9 | 137101455 | |||||||
chr9:137101699 | T | C | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+27T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137101699 | |||||||
chr9:137101741 | C | CTG | 4 | a0001c0001t0001g0022 a0001c0001t0001g0046 a0001c0025t0001g0130 others(1): Show |
7 | HG00673.hp1 HG02559.hp1 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.1254+83_1254+84dup others(2): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137101741 | ||||||
chr9:137101743 | G | C | 4 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0115 others(1): Show |
5 | HG01123.hp1 HG01255.hp2 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.1254+71G>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137101743 | |||||||
chr9:137101907 | G | A | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+235G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137101907 | |||||||
chr9:137101924 | TACAC | T | 36 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(33): Show |
46 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1254+256_1254+259d others(6): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137101924 | ||||||
chr9:137101934 | T | C | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+262T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137101934 | |||||||
chr9:137101966 | TACAC | T | 3 | a0001c0025t0001g0130 a0002c0009t0002g0104 a0002c0009t0002g0105 |
3 | HG01891.hp1 HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1254+298_1254+301d others(6): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137101966 | ||||||
chr9:137101986 | A | AGTACAGG others(31): Show |
2 | a0016c0028t0002g0129 a0017c0027t0002g0225 |
2 | HG03225.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1254+335_1254+336i others(40): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137101986 | ||||||
chr9:137101986 | A | AGTACAGG others(28): Show |
1 | a0006c0011t0002g0039 | 2 | NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1254+327_1254+328i others(37): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137101986 | ||||||
chr9:137102037 | T | C | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+365T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102037 | |||||||
chr9:137102046 | TAC | T | 3 | a0001c0001t0001g0042 a0001c0001t0001g0163 a0001c0001t0001g0210 |
4 | HG00639.hp1 HG00738.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.1254+380_1254+381d others(4): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102046 | ||||||
chr9:137102087 | A | C | 2 | a0002c0009t0002g0104 a0002c0009t0002g0105 |
2 | HG01891.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1254+415A>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102087 | |||||||
chr9:137102104 | C | T | 1 | a0001c0002t0002g0062 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1254+432C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102104 | |||||||
chr9:137102118 | T | TACAC | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+449_1254+450i others(6): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102118 | ||||||
chr9:137102189 | C | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(134): Show |
234 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.1254+517C>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102189 | |||||||
chr9:137102189 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1254+517C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102189 | |||||||
chr9:137102202 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1254+530C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102202 | |||||||
chr9:137102262 | T | TAGGTCGG others(2054): Show |
2 | a0002c0003t0002g0099 a0002c0012t0002g0098 |
2 | HG02055.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1254+616_1254+617i others(2063): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(2054): Show |
1 | a0002c0003t0002g0103 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1254+616_1254+617i others(2063): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(2054): Show |
1 | a0002c0003t0002g0106 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1254+616_1254+617i others(2063): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(2054): Show |
2 | a0002c0003t0002g0008 a0002c0003t0002g0109 |
8 | HG02109.hp1 HG02486.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1254+616_1254+617i others(2063): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(2050): Show |
1 | a0002c0003t0002g0107 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1254+616_1254+617i others(2059): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(2044): Show |
1 | a0002c0003t0002g0019 | 3 | HG02572.hp1 HG02723.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1254+616_1254+617i others(2053): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1666): Show |
1 | a0001c0001t0001g0165 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1254+616_1254+617i others(1675): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1666): Show |
1 | a0001c0001t0001g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1254+616_1254+617i others(1675): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(260): Show |
41 | a0001c0001t0001g0029 a0001c0002t0001g0003 a0001c0002t0001g0064 others(38): Show |
82 | HG00099.hp2 HG00423.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.1254+616_1254+617i others(269): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(260): Show |
1 | a0001c0002t0001g0083 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1254+616_1254+617i others(269): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1663): Show |
1 | a0001c0001t0001g0187 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1254+616_1254+617i others(1672): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(2062): Show |
2 | a0001c0001t0002g0015 a0008c0016t0002g0126 |
5 | HG00140.hp2 HG01346.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1254+616_1254+617i others(2071): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(2062): Show |
1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1254+616_1254+617i others(2071): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(2059): Show |
4 | a0001c0001t0002g0052 a0001c0001t0002g0116 a0001c0001t0002g0125 others(1): Show |
4 | HG03017.hp1 HG03491.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1254+616_1254+617i others(2068): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(2062): Show |
25 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(22): Show |
30 | HG00140.hp1 HG00642.hp2 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1254+616_1254+617i others(2071): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(3572): Show |
1 | a0001c0001t0002g0036 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1254+616_1254+617i others(3581): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(3572): Show |
1 | a0001c0001t0002g0034 | 2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1254+616_1254+617i others(3581): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(2867): Show |
1 | a0001c0001t0002g0110 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1254+616_1254+617i others(2876): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1663): Show |
1 | a0001c0001t0001g0181 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1254+616_1254+617i others(1672): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1666): Show |
1 | a0001c0001t0001g0202 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1254+616_1254+617i others(1675): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1666): Show |
1 | a0001c0001t0001g0172 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1254+616_1254+617i others(1675): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1666): Show |
1 | a0001c0001t0001g0166 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1254+616_1254+617i others(1675): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1666): Show |
2 | a0001c0001t0001g0022 a0001c0001t0001g0046 |
5 | HG00673.hp1 NA19004.hp1 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.1254+616_1254+617i others(1675): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1627): Show |
1 | a0002c0009t0002g0104 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1254+616_1254+617i others(1636): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1666): Show |
2 | a0001c0001t0001g0014 a0001c0001t0001g0219 |
6 | HG01106.hp1 HG02258.hp1 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+616_1254+617i others(1675): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1665): Show |
1 | a0001c0001t0001g0152 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1254+616_1254+617i others(1674): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1663): Show |
1 | a0001c0001t0001g0213 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1254+616_1254+617i others(1672): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1668): Show |
22 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0027 others(19): Show |
34 | HG00280.hp1 HG00558.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.1254+616_1254+617i others(1677): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1668): Show |
1 | a0001c0001t0001g0147 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1254+616_1254+617i others(1677): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1665): Show |
2 | a0001c0025t0001g0130 a0002c0009t0002g0105 |
2 | HG02280.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1254+616_1254+617i others(1674): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1666): Show |
80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(77): Show |
153 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.1254+616_1254+617i others(1675): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1662): Show |
5 | a0001c0001t0001g0133 a0001c0001t0001g0135 a0001c0001t0001g0168 others(2): Show |
5 | HG00597.hp2 HG02015.hp2 HG02040.hp1 others(2): Show |
intron_variant | MODIFIER | c.1254+616_1254+617i others(1671): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1663): Show |
1 | a0001c0001t0001g0137 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1254+616_1254+617i others(1672): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1668): Show |
1 | a0001c0001t0001g0040 | 2 | NA18939.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.1254+616_1254+617i others(1677): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1667): Show |
1 | a0001c0001t0001g0132 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1254+616_1254+617i others(1676): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1666): Show |
1 | a0001c0001t0001g0207 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1254+616_1254+617i others(1675): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1662): Show |
1 | a0001c0001t0001g0189 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1254+616_1254+617i others(1671): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1664): Show |
2 | a0004c0006t0001g0024 a0015c0026t0001g0151 |
4 | HG02886.hp2 HG02896.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+616_1254+617i others(1673): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1666): Show |
1 | a0001c0001t0001g0190 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1254+616_1254+617i others(1675): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1627): Show |
1 | a0001c0001t0001g0221 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1254+616_1254+617i others(1636): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1666): Show |
1 | a0001c0001t0001g0178 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1254+616_1254+617i others(1675): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1658): Show |
1 | a0001c0001t0001g0161 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1254+616_1254+617i others(1667): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(2018): Show |
2 | a0001c0001t0005g0012 a0001c0001t0005g0113 |
6 | HG02109.hp2 HG02809.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+616_1254+617i others(2027): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(1664): Show |
1 | a0001c0001t0001g0191 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1254+616_1254+617i others(1673): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTCGG others(2062): Show |
1 | a0001c0001t0002g0057 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1254+616_1254+617i others(2071): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | T | TAGGTGGT others(2040): Show |
3 | a0002c0003t0002g0091 a0002c0003t0002g0102 a0002c0003t0002g0108 |
3 | HG01891.hp2 HG02280.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1254+594_1254+595i others(2049): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102262 | TAGGTCGG others(384): Show |
T | 2 | a0006c0011t0002g0039 a0016c0028t0002g0129 |
3 | HG03225.hp2 NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1254+617_1254+1007 others(3): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102262 | ||||||
chr9:137102275 | T | G | 1 | a0017c0027t0002g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1254+603T>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102275 | |||||||
chr9:137102282 | C | CATTCACG others(2056): Show |
2 | a0005c0008t0002g0101 a0005c0013t0002g0096 |
2 | HG02630.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1254+616_1254+617i others(2065): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102282 | ||||||
chr9:137102282 | C | CATTCACG others(2060): Show |
2 | a0002c0003t0002g0020 a0002c0003t0002g0092 |
4 | HG02970.hp2 HG03579.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+616_1254+617i others(2069): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102282 | ||||||
chr9:137102282 | C | CATTCACG others(2060): Show |
1 | a0002c0003t0002g0100 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1254+616_1254+617i others(2069): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102282 | ||||||
chr9:137102282 | C | CATTCACG others(2052): Show |
1 | a0005c0008t0002g0093 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1254+616_1254+617i others(2061): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102282 | ||||||
chr9:137102285 | T | TCACGCTG others(189): Show |
1 | a0001c0001t0002g0055 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1254+616_1254+617i others(198): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102285 | ||||||
chr9:137102287 | A | ACGCTGTT others(269): Show |
1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+616_1254+617i others(278): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102287 | ||||||
chr9:137102287 | A | ACGCTGTT others(269): Show |
1 | a0002c0003t0001g0021 | 3 | HG01884.hp1 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+616_1254+617i others(278): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102287 | ||||||
chr9:137102288 | CTGTTGCA others(504): Show |
C | 1 | a0017c0027t0002g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1254+617_1254+1127 others(3): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102288 | |||||||
chr9:137102297 | G | A | 2 | a0001c0002t0002g0084 a0009c0014t0002g0082 |
2 | HG00558.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1254+625G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102297 | |||||||
chr9:137102298 | C | A | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+626C>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102298 | |||||||
chr9:137102301 | G | A | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+629G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102301 | |||||||
chr9:137102308 | G | A | 8 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0043 others(5): Show |
21 | HG00099.hp1 HG00735.hp1 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.1254+636G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102308 | |||||||
chr9:137102312 | G | C | 2 | a0001c0002t0002g0084 a0009c0014t0002g0082 |
2 | HG00558.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1254+640G>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102312 | |||||||
chr9:137102316 | T | TAC | 3 | a0001c0001t0002g0055 a0002c0003t0001g0021 a0002c0003t0002g0128 |
5 | HG01884.hp1 HG02055.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254+648_1254+649d others(4): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102316 | ||||||
chr9:137102318 | C | CACACATT others(370): Show |
2 | a0001c0002t0002g0084 a0009c0014t0002g0082 |
2 | HG00558.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1254+649_1254+650i others(379): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102318 | ||||||
chr9:137102326 | C | T | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+654C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102326 | |||||||
chr9:137102327 | G | A | 3 | a0001c0001t0002g0055 a0001c0002t0002g0084 a0009c0014t0002g0082 |
3 | HG00558.hp2 HG03704.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.1254+655G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102327 | |||||||
chr9:137102348 | G | A | 1 | a0002c0003t0002g0020 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1254+676G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102348 | |||||||
chr9:137102356 | T | TACACACA others(189): Show |
1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+687_1254+688i others(198): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102356 | ||||||
chr9:137102359 | A | ATTCACAC others(740): Show |
1 | a0002c0003t0001g0021 | 3 | HG01884.hp1 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+692_1254+693i others(749): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102359 | ||||||
chr9:137102364 | C | CACTGTTG others(35): Show |
1 | a0001c0001t0002g0055 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1254+692_1254+693i others(44): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102364 | |||||||
chr9:137102371 | G | A | 3 | a0001c0007t0001g0211 a0001c0007t0001g0212 a0001c0007t0001g0215 |
3 | HG01074.hp1 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1254+699G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102371 | |||||||
chr9:137102375 | A | G | 2 | a0001c0001t0002g0055 a0002c0003t0002g0128 |
2 | HG03704.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1254+703A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102375 | |||||||
chr9:137102382 | G | T | 4 | a0002c0003t0002g0019 a0002c0003t0002g0091 a0002c0003t0002g0102 others(1): Show |
6 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1254+710G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102382 | |||||||
chr9:137102386 | A | G | 7 | a0001c0001t0001g0145 a0001c0001t0002g0055 a0001c0001t0003g0004 others(4): Show |
10 | HG00558.hp1 HG01884.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1254+714A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102386 | |||||||
chr9:137102390 | C | G | 2 | a0001c0001t0002g0055 a0002c0003t0002g0128 |
2 | HG03704.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1254+718C>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102390 | |||||||
chr9:137102421 | T | C | 3 | a0001c0001t0002g0055 a0002c0003t0001g0021 a0002c0003t0002g0128 |
5 | HG01884.hp1 HG02055.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254+749T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102421 | |||||||
chr9:137102438 | C | T | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+766C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102438 | |||||||
chr9:137102439 | A | ACTTGCAG others(449): Show |
1 | a0002c0003t0001g0021 | 3 | HG01884.hp1 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+769_1254+770i others(458): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102439 | ||||||
chr9:137102439 | A | G | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+767A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102439 | |||||||
chr9:137102440 | CTG | C | 17 | a0002c0003t0002g0008 a0002c0003t0002g0019 a0002c0003t0002g0020 others(14): Show |
27 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1254+770_1254+771d others(4): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102440 | ||||||
chr9:137102450 | C | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0139 a0001c0001t0001g0185 others(1): Show |
5 | HG00738.hp2 HG01192.hp1 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1254+778C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102450 | |||||||
chr9:137102478 | C | A | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+806C>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102478 | |||||||
chr9:137102479 | ATT | A | 2 | a0001c0001t0002g0055 a0002c0003t0001g0021 |
4 | HG01884.hp1 HG02055.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+808_1254+809d others(4): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102479 | |||||||
chr9:137102480 | T | C | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+808T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102480 | |||||||
chr9:137102481 | T | G | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(187): Show |
305 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(302): Show |
intron_variant | MODIFIER | c.1254+809T>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102481 | |||||||
chr9:137102483 | T | A | 1 | a0001c0001t0002g0055 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1254+811T>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102483 | |||||||
chr9:137102484 | G | C | 1 | a0001c0001t0002g0055 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1254+812G>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102484 | |||||||
chr9:137102502 | A | G | 3 | a0001c0001t0002g0055 a0002c0003t0001g0021 a0002c0003t0002g0128 |
5 | HG01884.hp1 HG02055.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254+830A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102502 | |||||||
chr9:137102504 | T | TG | 1 | a0002c0003t0001g0021 | 3 | HG01884.hp1 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+833dupG | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102504 | ||||||
chr9:137102506 | T | G | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+834T>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102506 | |||||||
chr9:137102507 | T | G | 1 | a0002c0003t0001g0021 | 3 | HG01884.hp1 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+835T>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102507 | |||||||
chr9:137102508 | A | T | 1 | a0002c0003t0001g0021 | 3 | HG01884.hp1 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+836A>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102508 | |||||||
chr9:137102509 | C | T | 1 | a0002c0003t0001g0021 | 3 | HG01884.hp1 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+837C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102509 | |||||||
chr9:137102519 | C | T | 2 | a0001c0001t0002g0055 a0002c0003t0002g0128 |
2 | HG03704.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1254+847C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102519 | |||||||
chr9:137102540 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1254+868C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102540 | |||||||
chr9:137102549 | TACAC | T | 37 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(34): Show |
49 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(46): Show |
intron_variant | MODIFIER | c.1254+881_1254+884d others(6): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102549 | ||||||
chr9:137102559 | C | A | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+887C>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102559 | |||||||
chr9:137102565 | G | GTTGCAGG others(767): Show |
1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+899_1254+900i others(776): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102565 | ||||||
chr9:137102572 | A | G | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+900A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102572 | |||||||
chr9:137102573 | T | C | 2 | a0002c0003t0001g0021 a0002c0003t0002g0128 |
4 | HG01884.hp1 HG02055.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+901T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102573 | |||||||
chr9:137102577 | C | G | 2 | a0001c0001t0005g0012 a0001c0001t0005g0113 |
6 | HG02109.hp2 HG02809.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1254+905C>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102577 | |||||||
chr9:137102583 | G | A | 1 | a0002c0003t0001g0021 | 3 | HG01884.hp1 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+911G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102583 | |||||||
chr9:137102587 | C | T | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+915C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102587 | |||||||
chr9:137102594 | ATT | A | 1 | a0002c0003t0001g0021 | 3 | HG01884.hp1 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+923_1254+924d others(4): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102594 | |||||||
chr9:137102595 | T | C | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+923T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102595 | |||||||
chr9:137102599 | C | T | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+927C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102599 | |||||||
chr9:137102609 | A | G | 2 | a0002c0003t0001g0021 a0002c0003t0002g0128 |
4 | HG01884.hp1 HG02055.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+937A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102609 | |||||||
chr9:137102620 | C | T | 1 | a0002c0003t0001g0021 | 3 | HG01884.hp1 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+948C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102620 | |||||||
chr9:137102629 | T | TACATTCA others(74): Show |
1 | a0002c0003t0001g0021 | 3 | HG01884.hp1 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+965_1254+966i others(83): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102629 | ||||||
chr9:137102639 | C | G | 1 | a0001c0001t0001g0022 | 2 | NA19060.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1254+967C>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102639 | |||||||
chr9:137102646 | T | A | 2 | a0002c0003t0001g0021 a0002c0003t0002g0128 |
4 | HG01884.hp1 HG02055.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+974T>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102646 | |||||||
chr9:137102649 | C | T | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+977C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102649 | |||||||
chr9:137102666 | T | G | 2 | a0006c0011t0002g0039 a0016c0028t0002g0129 |
3 | HG03225.hp2 NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1254+994T>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102666 | |||||||
chr9:137102667 | TACAC | T | 4 | a0001c0002t0002g0006 a0001c0002t0002g0085 a0001c0002t0002g0087 others(1): Show |
4 | HG02040.hp2 HG02056.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1254+999_1254+1002 others(7): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102667 | ||||||
chr9:137102680 | A | G | 4 | a0002c0003t0001g0021 a0002c0003t0002g0128 a0006c0011t0002g0039 others(1): Show |
7 | HG01884.hp1 HG02055.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1254+1008A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102680 | |||||||
chr9:137102690 | A | G | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+1018A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102690 | |||||||
chr9:137102691 | C | T | 2 | a0002c0003t0001g0021 a0016c0028t0002g0129 |
4 | HG01884.hp1 HG02055.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+1019C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102691 | |||||||
chr9:137102692 | A | G | 4 | a0002c0003t0001g0021 a0002c0003t0002g0128 a0006c0011t0002g0039 others(1): Show |
7 | HG01884.hp1 HG02055.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1254+1020A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102692 | |||||||
chr9:137102695 | C | T | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+1023C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102695 | |||||||
chr9:137102705 | C | G | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+1033C>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102705 | |||||||
chr9:137102708 | T | G | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+1036T>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102708 | |||||||
chr9:137102709 | TACAC | T | 1 | a0002c0003t0001g0021 | 3 | HG01884.hp1 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+1041_1254+104 others(8): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102709 | ||||||
chr9:137102721 | T | C | 1 | a0002c0003t0001g0021 | 3 | HG01884.hp1 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+1049T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102721 | |||||||
chr9:137102731 | G | A | 1 | a0002c0003t0001g0021 | 3 | HG01884.hp1 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+1059G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102731 | |||||||
chr9:137102733 | C | A | 3 | a0002c0003t0002g0128 a0006c0011t0002g0039 a0016c0028t0002g0129 |
4 | HG03225.hp2 HG06807.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+1061C>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102733 | |||||||
chr9:137102734 | G | C | 1 | a0001c0002t0002g0006 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1254+1062G>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102734 | |||||||
chr9:137102736 | G | A | 3 | a0002c0003t0002g0128 a0006c0011t0002g0039 a0016c0028t0002g0129 |
4 | HG03225.hp2 HG06807.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+1064G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102736 | |||||||
chr9:137102752 | ACATTCAC others(37): Show |
A | 2 | a0006c0011t0002g0039 a0016c0028t0002g0129 |
3 | HG03225.hp2 NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1254+1084_1254+112 others(48): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102752 | ||||||
chr9:137102760 | A | G | 1 | a0002c0003t0001g0021 | 3 | HG01884.hp1 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+1088A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102760 | |||||||
chr9:137102761 | C | CTG | 2 | a0002c0003t0001g0021 a0002c0003t0002g0128 |
4 | HG01884.hp1 HG02055.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+1090_1254+109 others(6): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102761 | ||||||
chr9:137102766 | A | T | 1 | a0002c0003t0001g0021 | 3 | HG01884.hp1 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+1094A>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102766 | |||||||
chr9:137102782 | G | GGTTACAT others(480): Show |
1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+1112_1254+111 others(491): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102782 | ||||||
chr9:137102799 | T | C | 2 | a0002c0003t0001g0021 a0002c0003t0002g0128 |
4 | HG01884.hp1 HG02055.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+1127T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102799 | |||||||
chr9:137102800 | G | A | 1 | a0002c0003t0001g0021 | 3 | HG01884.hp1 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+1128G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102800 | |||||||
chr9:137102810 | G | A | 2 | a0002c0003t0001g0021 a0017c0027t0002g0225 |
4 | HG01884.hp1 HG02055.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+1138G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102810 | |||||||
chr9:137102811 | C | T | 2 | a0006c0011t0002g0039 a0016c0028t0002g0129 |
3 | HG03225.hp2 NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1254+1139C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102811 | |||||||
chr9:137102812 | G | A | 1 | a0002c0003t0001g0021 | 3 | HG01884.hp1 HG02055.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1254+1140G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102812 | |||||||
chr9:137102822 | G | C | 1 | a0001c0002t0002g0075 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1254+1150G>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102822 | |||||||
chr9:137102825 | G | C | 2 | a0002c0003t0001g0021 a0017c0027t0002g0225 |
4 | HG01884.hp1 HG02055.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+1153G>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102825 | |||||||
chr9:137102828 | T | G | 2 | a0006c0011t0002g0039 a0016c0028t0002g0129 |
3 | HG03225.hp2 NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1254+1156T>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102828 | |||||||
chr9:137102841 | C | T | 38 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(35): Show |
50 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.1254+1169C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102841 | |||||||
chr9:137102842 | A | G | 41 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(38): Show |
54 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(51): Show |
intron_variant | MODIFIER | c.1254+1170A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102842 | |||||||
chr9:137102843 | C | G | 36 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(33): Show |
46 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1254+1171C>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102843 | |||||||
chr9:137102845 | G | T | 2 | a0006c0011t0002g0039 a0016c0028t0002g0129 |
3 | HG03225.hp2 NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1254+1173G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102845 | |||||||
chr9:137102851 | G | GATGTGCA others(31): Show |
1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+1179_1254+118 others(42): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102851 | |||||||
chr9:137102853 | C | A | 1 | a0017c0027t0002g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1254+1181C>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102853 | |||||||
chr9:137102856 | G | A | 1 | a0017c0027t0002g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1254+1184G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102856 | |||||||
chr9:137102879 | T | C | 3 | a0002c0003t0002g0128 a0006c0011t0002g0039 a0016c0028t0002g0129 |
4 | HG03225.hp2 HG06807.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+1207T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102879 | |||||||
chr9:137102891 | C | T | 1 | a0017c0027t0002g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1254+1219C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102891 | |||||||
chr9:137102892 | G | A | 2 | a0006c0011t0002g0039 a0016c0028t0002g0129 |
3 | HG03225.hp2 NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1254+1220G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102892 | |||||||
chr9:137102897 | G | C | 1 | a0001c0001t0002g0110 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1254+1225G>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102897 | |||||||
chr9:137102901 | A | G | 4 | a0002c0003t0002g0128 a0006c0011t0002g0039 a0016c0028t0002g0129 others(1): Show |
5 | HG03225.hp2 HG03471.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254+1229A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102901 | |||||||
chr9:137102908 | T | G | 1 | a0017c0027t0002g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1254+1236T>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102908 | |||||||
chr9:137102909 | TAC | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(131): Show |
231 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1254+1243_1254+124 others(6): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102909 | ||||||
chr9:137102916 | ATTCACGC others(458): Show |
A | 2 | a0006c0011t0002g0039 a0016c0028t0002g0129 |
3 | HG03225.hp2 NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1254+1245_1254+170 others(4): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102916 | |||||||
chr9:137102921 | CGCTGTTG others(455): Show |
C | 1 | a0017c0027t0002g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1254+1262_1254+172 others(4): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137102921 | ||||||
chr9:137102922 | G | A | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+1250G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102922 | |||||||
chr9:137102932 | G | A | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+1260G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102932 | |||||||
chr9:137102934 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(190): Show |
314 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(311): Show |
intron_variant | MODIFIER | c.1254+1262A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102934 | |||||||
chr9:137102947 | G | C | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+1275G>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102947 | |||||||
chr9:137102963 | C | T | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+1291C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102963 | |||||||
chr9:137102967 | T | G | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+1295T>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102967 | |||||||
chr9:137102976 | G | T | 1 | a0001c0002t0002g0051 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1254+1304G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102976 | |||||||
chr9:137102991 | C | G | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+1319C>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137102991 | |||||||
chr9:137103001 | T | C | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+1329T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103001 | |||||||
chr9:137103002 | A | ACTGTTGC others(375): Show |
1 | a0001c0005t0004g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1254+1594_1254+159 others(386): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137103002 | ||||||
chr9:137103039 | C | T | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+1367C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103039 | |||||||
chr9:137103040 | A | G | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+1368A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103040 | |||||||
chr9:137103084 | C | T | 4 | a0002c0003t0002g0019 a0002c0003t0002g0091 a0002c0003t0002g0102 others(1): Show |
6 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1254+1412C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103084 | |||||||
chr9:137103110 | C | T | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+1438C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103110 | |||||||
chr9:137103111 | A | T | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+1439A>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103111 | |||||||
chr9:137103140 | GTGT | G | 4 | a0002c0003t0002g0019 a0002c0003t0002g0091 a0002c0003t0002g0102 others(1): Show |
6 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1254+1470_1254+147 others(7): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137103140 | ||||||
chr9:137103174 | G | A | 1 | a0001c0001t0007g0154 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1254+1502G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103174 | |||||||
chr9:137103178 | G | T | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1254+1506G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103178 | |||||||
chr9:137103193 | CTG | C | 18 | a0002c0003t0002g0008 a0002c0003t0002g0019 a0002c0003t0002g0020 others(15): Show |
28 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.1254+1523_1254+152 others(6): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137103193 | ||||||
chr9:137103204 | G | A | 1 | a0001c0001t0001g0216 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1254+1532G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103204 | |||||||
chr9:137103220 | T | G | 1 | a0001c0002t0001g0003 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1254+1548T>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103220 | |||||||
chr9:137103254 | C | T | 2 | a0001c0001t0002g0222 a0001c0001t0002g0223 |
2 | HG03834.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1254+1582C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103254 | |||||||
chr9:137103265 | A | ACGTGCTG others(108): Show |
1 | a0001c0001t0001g0115 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1254+1594_1254+159 others(119): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137103265 | ||||||
chr9:137103267 | A | G | 35 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(32): Show |
45 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.1254+1595A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103267 | |||||||
chr9:137103280 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1254+1608C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103280 | |||||||
chr9:137103383 | T | C | 2 | a0006c0011t0002g0039 a0016c0028t0002g0129 |
3 | HG03225.hp2 NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1254+1711T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103383 | |||||||
chr9:137103387 | G | T | 1 | a0017c0027t0002g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1254+1715G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103387 | |||||||
chr9:137103426 | G | T | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+1754G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103426 | |||||||
chr9:137103482 | A | G | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+1810A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103482 | |||||||
chr9:137103511 | C | T | 1 | a0002c0003t0002g0109 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1254+1839C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103511 | |||||||
chr9:137103512 | G | A | 3 | a0001c0007t0001g0211 a0001c0007t0001g0212 a0001c0007t0001g0215 |
3 | HG01074.hp1 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1254+1840G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103512 | |||||||
chr9:137103519 | C | T | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+1847C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103519 | |||||||
chr9:137103537 | C | T | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+1865C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103537 | |||||||
chr9:137103557 | T | TTGGTGTT others(112): Show |
1 | a0001c0001t0001g0169 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1254+1917_1254+191 others(123): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137103557 | ||||||
chr9:137103566 | C | T | 1 | a0016c0028t0002g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1254+1894C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103566 | |||||||
chr9:137103578 | C | CTTGCAGG others(35): Show |
1 | a0001c0001t0003g0148 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1254+1917_1254+191 others(46): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137103578 | ||||||
chr9:137103581 | G | A | 1 | a0001c0002t0002g0087 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1254+1909G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103581 | |||||||
chr9:137103587 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1254+1915G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103587 | |||||||
chr9:137103590 | C | T | 136 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(133): Show |
233 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(230): Show |
intron_variant | MODIFIER | c.1254+1918C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103590 | |||||||
chr9:137103591 | G | A | 1 | a0001c0001t0003g0148 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1254+1919G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103591 | |||||||
chr9:137103628 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1254+1956C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103628 | |||||||
chr9:137103637 | C | T | 53 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(50): Show |
73 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.1254+1965C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103637 | |||||||
chr9:137103643 | TACAC | T | 2 | a0001c0001t0001g0037 a0001c0001t0001g0131 |
3 | NA18963.hp1 NA18987.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.1254+1975_1254+197 others(8): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137103643 | ||||||
chr9:137103666 | G | A | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | NA18944.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.1254+1994G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103666 | |||||||
chr9:137103707 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1254+2035C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103707 | |||||||
chr9:137103708 | G | A | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+2036G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103708 | |||||||
chr9:137103717 | C | T | 1 | a0006c0011t0002g0039 | 2 | NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1254+2045C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103717 | |||||||
chr9:137103725 | TACAC | T | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+2057_1254+206 others(8): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137103725 | ||||||
chr9:137103733 | T | C | 1 | a0001c0001t0002g0110 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1254+2061T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103733 | |||||||
chr9:137103746 | GTGCAGGT others(232): Show |
G | 1 | a0001c0001t0001g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1254+2100_1255-211 others(4): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137103746 | ||||||
chr9:137103792 | T | C | 4 | a0001c0002t0002g0006 a0001c0002t0002g0066 a0001c0002t0002g0067 others(1): Show |
11 | HG00621.hp2 HG02040.hp2 HG02083.hp2 others(8): Show |
intron_variant | MODIFIER | c.1254+2120T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103792 | |||||||
chr9:137103802 | C | T | 1 | a0001c0001t0002g0110 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1254+2130C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103802 | |||||||
chr9:137103832 | G | A | 1 | a0002c0003t0002g0020 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1254+2160G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103832 | |||||||
chr9:137103872 | A | G | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1254+2200A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103872 | |||||||
chr9:137103880 | TACAC | T | 4 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0203 others(1): Show |
5 | HG00735.hp2 HG02630.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1254+2212_1254+221 others(8): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137103880 | ||||||
chr9:137103944 | C | T | 1 | a0016c0028t0002g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1255-2181C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137103944 | |||||||
chr9:137104028 | G | A | 36 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(33): Show |
46 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1255-2097G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104028 | |||||||
chr9:137104031 | C | T | 2 | a0001c0001t0005g0012 a0001c0001t0005g0113 |
6 | HG02109.hp2 HG02809.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.1255-2094C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104031 | |||||||
chr9:137104088 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1255-2037C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104088 | |||||||
chr9:137104105 | G | T | 1 | a0016c0028t0002g0129 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1255-2020G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104105 | |||||||
chr9:137104171 | T | C | 1 | a0001c0001t0001g0173 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1255-1954T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104171 | |||||||
chr9:137104225 | G | A | 36 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(33): Show |
46 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(43): Show |
intron_variant | MODIFIER | c.1255-1900G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104225 | |||||||
chr9:137104241 | G | T | 194 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(191): Show |
311 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(308): Show |
intron_variant | MODIFIER | c.1255-1884G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104241 | |||||||
chr9:137104280 | G | A | 137 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(134): Show |
234 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(231): Show |
intron_variant | MODIFIER | c.1255-1845G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104280 | |||||||
chr9:137104297 | G | A | 6 | a0001c0002t0002g0030 a0001c0002t0002g0051 a0001c0002t0002g0062 others(3): Show |
7 | NA18942.hp2 NA18965.hp1 NA18977.hp2 others(4): Show |
intron_variant | MODIFIER | c.1255-1828G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104297 | |||||||
chr9:137104304 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1255-1821C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104304 | |||||||
chr9:137104311 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1255-1814C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104311 | |||||||
chr9:137104459 | T | C | 1 | a0001c0002t0002g0068 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1255-1666T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104459 | |||||||
chr9:137104460 | C | T | 1 | a0001c0002t0002g0068 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1255-1665C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104460 | |||||||
chr9:137104480 | G | A | 1 | a0017c0027t0002g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1255-1645G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104480 | |||||||
chr9:137104628 | C | T | 1 | a0006c0011t0002g0039 | 2 | NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1255-1497C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104628 | |||||||
chr9:137104632 | G | A | 1 | a0006c0011t0002g0039 | 2 | NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1255-1493G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104632 | |||||||
chr9:137104636 | C | T | 3 | a0001c0007t0001g0211 a0001c0007t0001g0212 a0001c0007t0001g0215 |
3 | HG01074.hp1 HG02647.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1255-1489C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104636 | |||||||
chr9:137104661 | T | C | 3 | a0002c0003t0002g0128 a0006c0011t0002g0039 a0016c0028t0002g0129 |
4 | HG03225.hp2 HG06807.hp2 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1464T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104661 | |||||||
chr9:137104720 | G | A | 4 | a0001c0025t0001g0130 a0006c0011t0002g0039 a0016c0028t0002g0129 others(1): Show |
5 | HG02559.hp1 HG03225.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1255-1405G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104720 | |||||||
chr9:137104724 | G | A | 1 | a0006c0011t0002g0039 | 2 | NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1255-1401G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104724 | |||||||
chr9:137104729 | A | C | 10 | a0001c0001t0001g0111 a0001c0001t0001g0152 a0001c0001t0001g0153 others(7): Show |
12 | HG01074.hp1 HG01891.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1255-1396A>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104729 | |||||||
chr9:137104779 | TCTG | T | 5 | a0002c0009t0002g0104 a0002c0009t0002g0105 a0006c0011t0002g0039 others(2): Show |
6 | HG01891.hp1 HG02280.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.1255-1343_1255-134 others(7): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137104779 | ||||||
chr9:137104822 | G | C | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1303G>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104822 | |||||||
chr9:137104833 | G | A | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1292G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104833 | |||||||
chr9:137104853 | CACCTGCC others(43): Show |
C | 1 | a0001c0001t0003g0148 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1255-1271_1255-122 others(54): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104853 | |||||||
chr9:137104868 | G | C | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1257G>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104868 | |||||||
chr9:137104871 | T | C | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1254T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104871 | |||||||
chr9:137104873 | T | C | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1252T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104873 | |||||||
chr9:137104876 | G | C | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1249G>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104876 | |||||||
chr9:137104877 | G | T | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1248G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104877 | |||||||
chr9:137104879 | G | C | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1246G>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104879 | |||||||
chr9:137104882 | G | T | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1243G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104882 | |||||||
chr9:137104887 | TGTGGG | T | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1237_1255-123 others(9): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104887 | |||||||
chr9:137104893 | T | A | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1232T>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104893 | |||||||
chr9:137104897 | C | G | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1228C>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104897 | |||||||
chr9:137104899 | C | A | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1226C>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104899 | |||||||
chr9:137104899 | CACCT | C | 25 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0027 others(22): Show |
40 | HG00280.hp1 HG00558.hp1 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1255-1225_1255-122 others(8): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104899 | |||||||
chr9:137104900 | A | ATGGAATC others(321): Show |
3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1225_1255-122 others(332): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104900 | |||||||
chr9:137104903 | T | A | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1222T>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104903 | |||||||
chr9:137104905 | C | G | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1220C>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104905 | |||||||
chr9:137104907 | T | TG | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1217dupG | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137104907 | ||||||
chr9:137104910 | G | GA | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1215_1255-121 others(5): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104910 | |||||||
chr9:137104913 | T | A | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1212T>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104913 | |||||||
chr9:137104919 | G | A | 2 | a0001c0001t0007g0154 a0001c0001t0007g0155 |
2 | HG03041.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1255-1206G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137104919 | |||||||
chr9:137105015 | C | G | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1110C>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105015 | |||||||
chr9:137105015 | C | T | 3 | a0001c0005t0004g0118 a0001c0005t0004g0119 a0001c0005t0004g0120 |
3 | HG00642.hp2 HG01175.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.1255-1110C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105015 | |||||||
chr9:137105017 | T | C | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-1108T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105017 | |||||||
chr9:137105284 | C | T | 1 | a0017c0027t0002g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1255-841C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105284 | |||||||
chr9:137105308 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1255-817C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105308 | |||||||
chr9:137105331 | CCACACCA others(17): Show |
C | 1 | a0001c0001t0001g0190 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.1255-790_1255-767d others(26): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137105331 | ||||||
chr9:137105335 | A | ACCATCCA others(17): Show |
2 | a0006c0011t0002g0039 a0016c0028t0002g0129 |
3 | HG03225.hp2 NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1255-774_1255-773i others(26): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137105335 | ||||||
chr9:137105335 | ACCATCCA others(17): Show |
A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(106): Show |
187 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(184): Show |
intron_variant | MODIFIER | c.1255-769_1255-746d others(26): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr9 | 137105335 | ||||||
chr9:137105367 | C | T | 1 | a0001c0001t0001g0214 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1255-758C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105367 | |||||||
chr9:137105436 | T | C | 17 | a0002c0003t0002g0008 a0002c0003t0002g0019 a0002c0003t0002g0020 others(14): Show |
27 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1255-689T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105436 | |||||||
chr9:137105437 | G | A | 7 | a0002c0003t0002g0008 a0002c0003t0002g0099 a0002c0003t0002g0103 others(4): Show |
13 | HG01243.hp2 HG02055.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.1255-688G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105437 | |||||||
chr9:137105452 | A | T | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1255-673A>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105452 | |||||||
chr9:137105457 | G | C | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-668G>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105457 | |||||||
chr9:137105473 | C | A | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-652C>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105473 | |||||||
chr9:137105474 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0178 |
2 | NA18939.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.1255-651G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105474 | |||||||
chr9:137105494 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1255-631C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105494 | |||||||
chr9:137105613 | C | T | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1255-512C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105613 | |||||||
chr9:137105630 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1255-495G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105630 | |||||||
chr9:137105663 | C | T | 138 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(135): Show |
236 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.1255-462C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105663 | |||||||
chr9:137105705 | A | G | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-420A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105705 | |||||||
chr9:137105804 | G | A | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-321G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105804 | |||||||
chr9:137105871 | T | C | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-254T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105871 | |||||||
chr9:137105895 | C | T | 16 | a0002c0003t0002g0008 a0002c0003t0002g0019 a0002c0003t0002g0020 others(13): Show |
26 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.1255-230C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105895 | |||||||
chr9:137105921 | G | A | 5 | a0001c0001t0001g0010 a0001c0001t0001g0153 a0001c0007t0001g0211 others(2): Show |
10 | HG01074.hp1 HG02647.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1255-204G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105921 | |||||||
chr9:137105951 | A | G | 3 | a0006c0011t0002g0039 a0016c0028t0002g0129 a0017c0027t0002g0225 |
4 | HG03225.hp2 HG03471.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.1255-174A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105951 | |||||||
chr9:137105975 | A | G | 4 | a0001c0001t0002g0110 a0006c0011t0002g0039 a0016c0028t0002g0129 others(1): Show |
5 | HG02258.hp2 HG03225.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1255-150A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137105975 | |||||||
chr9:137106003 | T | C | 1 | a0001c0001t0001g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1255-122T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137106003 | |||||||
chr9:137106089 | T | C | 5 | a0001c0002t0002g0030 a0001c0002t0002g0088 a0006c0011t0002g0039 others(2): Show |
7 | HG03225.hp2 HG03471.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1255-36T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137106089 | |||||||
chr9:137106092 | C | G | 5 | a0001c0002t0002g0030 a0001c0002t0002g0088 a0006c0011t0002g0039 others(2): Show |
7 | HG03225.hp2 HG03471.hp1 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1255-33C>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137106092 | |||||||
chr9:137106120 | C | T | 1 | a0004c0006t0001g0024 | 3 | HG02886.hp2 HG03098.hp2 NA19240.hp1 |
splice_region_variant&intron_variant | LOW | c.1255-5C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 8/12 | chr9 | 137106120 | |||||||
chr9:137106325 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1445+10G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 9/12 | chr9 | 137106325 | |||||||
chr9:137106345 | C | T | 1 | a0001c0002t0002g0081 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1445+30C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 9/12 | chr9 | 137106345 | |||||||
chr9:137106346 | G | A | 1 | a0001c0001t0002g0053 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1445+31G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 9/12 | chr9 | 137106346 | |||||||
chr9:137106420 | G | A | 8 | a0001c0001t0001g0152 a0002c0003t0002g0008 a0002c0003t0002g0099 others(5): Show |
14 | HG01243.hp2 HG02055.hp2 HG02056.hp1 others(11): Show |
intron_variant | MODIFIER | c.1445+105G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 9/12 | chr9 | 137106420 | |||||||
chr9:137106581 | G | A | 1 | a0001c0002t0002g0078 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1446-108G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 9/12 | chr9 | 137106581 | |||||||
chr9:137106584 | C | T | 1 | a0002c0003t0001g0095 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1446-105C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 9/12 | chr9 | 137106584 | |||||||
chr9:137106618 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0165 a0001c0001t0001g0199 |
5 | NA18950.hp1 NA18970.hp1 NA18974.hp2 others(2): Show |
intron_variant | MODIFIER | c.1446-71G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 9/12 | chr9 | 137106618 | |||||||
chr9:137106623 | T | G | 1 | a0001c0005t0004g0118 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1446-66T>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 9/12 | chr9 | 137106623 | |||||||
chr9:137106632 | C | T | 2 | a0001c0001t0001g0032 a0001c0001t0002g0032 |
2 | HG01123.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1446-57C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 9/12 | chr9 | 137106632 | |||||||
chr9:137106640 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG00741.hp1 HG01928.hp1 |
intron_variant | MODIFIER | c.1446-49G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 9/12 | chr9 | 137106640 | |||||||
chr9:137106652 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1446-37C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 9/12 | chr9 | 137106652 | |||||||
chr9:137106823 | C | T | 1 | a0006c0011t0002g0039 | 2 | NA18978.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.1566+14C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 10/12 | chr9 | 137106823 | |||||||
chr9:137106842 | C | T | 4 | a0002c0003t0002g0019 a0002c0003t0002g0091 a0002c0003t0002g0102 others(1): Show |
6 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1566+33C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 10/12 | chr9 | 137106842 | |||||||
chr9:137106877 | T | C | 4 | a0002c0003t0002g0019 a0002c0003t0002g0091 a0002c0003t0002g0102 others(1): Show |
6 | HG01891.hp2 HG02280.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1566+68T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 10/12 | chr9 | 137106877 | |||||||
chr9:137106878 | G | T | 1 | a0001c0001t0002g0110 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1566+69G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 10/12 | chr9 | 137106878 | |||||||
chr9:137106889 | G | GAAC | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(193): Show |
319 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(316): Show |
intron_variant | MODIFIER | c.1566+81_1566+83dup others(3): Show |
MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr9 | 137106889 | ||||||
chr9:137107036 | C | T | 1 | a0001c0001t0002g0114 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1567-214C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 10/12 | chr9 | 137107036 | |||||||
chr9:137107124 | C | T | 17 | a0002c0003t0002g0008 a0002c0003t0002g0019 a0002c0003t0002g0020 others(14): Show |
27 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.1567-126C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 10/12 | chr9 | 137107124 | |||||||
chr9:137107232 | G | A | 1 | a0001c0002t0002g0076 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1567-18G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 10/12 | chr9 | 137107232 | |||||||
chr9:137107526 | C | A | 36 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(33): Show |
46 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(43): Show |
splice_region_variant&intron_variant | LOW | c.1765-5C>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 11/12 | chr9 | 137107526 | |||||||
chr9:137107669 | A | G | 1 | a0017c0027t0002g0225 | 1 | HG03471.hp1 | splice_region_variant&intron_variant | LOW | c.1896+7A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 12/12 | chr9 | 137107669 | |||||||
chr9:137107684 | G | A | 12 | a0001c0001t0002g0222 a0001c0001t0002g0223 a0001c0002t0002g0011 others(9): Show |
17 | HG00609.hp1 HG01167.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.1896+22G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 12/12 | chr9 | 137107684 | |||||||
chr9:137107693 | C | T | 1 | a0017c0027t0002g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1896+31C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 12/12 | chr9 | 137107693 | |||||||
chr9:137107701 | G | A | 1 | a0001c0002t0002g0079 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1896+39G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 12/12 | chr9 | 137107701 | |||||||
chr9:137107727 | G | A | 18 | a0001c0001t0002g0110 a0002c0003t0002g0008 a0002c0003t0002g0019 others(15): Show |
28 | HG01243.hp2 HG01891.hp2 HG02055.hp2 others(25): Show |
intron_variant | MODIFIER | c.1896+65G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 12/12 | chr9 | 137107727 | |||||||
chr9:137107735 | C | T | 55 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(52): Show |
75 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1896+73C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 12/12 | chr9 | 137107735 | |||||||
chr9:137107768 | A | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(193): Show |
315 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.1896+106A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 12/12 | chr9 | 137107768 | |||||||
chr9:137107771 | C | T | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1896+109C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 12/12 | chr9 | 137107771 | |||||||
chr9:137107809 | A | G | 35 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(32): Show |
45 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.1896+147A>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 12/12 | chr9 | 137107809 | |||||||
chr9:137107892 | C | T | 1 | a0017c0027t0002g0225 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1896+230C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 12/12 | chr9 | 137107892 | |||||||
chr9:137107894 | C | G | 1 | a0001c0001t0002g0112 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1896+232C>G | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 12/12 | chr9 | 137107894 | |||||||
chr9:137108049 | T | C | 198 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(195): Show |
321 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.1897-339T>C | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 12/12 | chr9 | 137108049 | |||||||
chr9:137108115 | C | A | 15 | a0002c0003t0002g0008 a0002c0003t0002g0019 a0002c0003t0002g0020 others(12): Show |
25 | HG01243.hp2 HG02055.hp2 HG02056.hp1 others(22): Show |
intron_variant | MODIFIER | c.1897-273C>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 12/12 | chr9 | 137108115 | |||||||
chr9:137108171 | G | A | 1 | a0001c0002t0002g0080 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1897-217G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 12/12 | chr9 | 137108171 | |||||||
chr9:137108178 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1897-210G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 12/12 | chr9 | 137108178 | |||||||
chr9:137108246 | G | T | 1 | a0002c0003t0002g0128 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1897-142G>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 12/12 | chr9 | 137108246 | |||||||
chr9:137108264 | G | A | 1 | a0001c0005t0004g0119 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1897-124G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 12/12 | chr9 | 137108264 | |||||||
chr9:137108302 | C | T | 35 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(32): Show |
45 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.1897-86C>T | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 12/12 | chr9 | 137108302 | |||||||
chr9:137108367 | G | A | 1 | a0001c0001t0001g0188 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1897-21G>A | MAN1B1 | ENSG00000177239.16 | transcript | ENST00000371589.9 | protein_coding | 12/12 | chr9 | 137108367 |