Item | Value |
---|---|
geneid | 701 |
ensemblid | ENSG00000156970.13 |
hgncid | 1149 |
symbol | BUB1B |
name | BUB1 mitotic checkpoint serine/threonine kinase B |
refseq_nuc | NM_001211.6 |
refseq_prot | NP_001202.5 |
ensembl_nuc | ENST00000287598.11 |
ensembl_prot | ENSP00000287598.7 |
mane_status | MANE Select |
chr | chr15 |
start | 40161069 |
end | 40221123 |
strand | + |
ver | v1.2 |
region | chr15:40161069-40221123 |
region5000 | chr15:40156069-40226123 |
regionname0 | BUB1B_chr15_40161069_40221123 |
regionname5000 | BUB1B_chr15_40156069_40226123 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1050 | 177 | 34 | 28 | 79 | 10 | 26 | 64 | BUB1B_chr15_40156069_40226123 | BUB1B | MAAVK others(1045): Show |
chr15 | 40156069 | 40226123 |
a0002 | 1/1 | 1050 | 121 | 11 | 24 | 70 | 2 | 12 | 53 | BUB1B_chr15_40156069_40226123 | BUB1B | MAAVK others(1045): Show |
chr15 | 40156069 | 40226123 |
a0003 | 0/0 | 1050 | 28 | 27 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | MAAVK others(1045): Show |
chr15 | 40156069 | 40226123 |
a0004 | 0/0 | 1050 | 9 | 8 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | MAAVK others(1045): Show |
chr15 | 40156069 | 40226123 |
a0005 | 0/0 | 1050 | 9 | 7 | 2 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | MAAVK others(1045): Show |
chr15 | 40156069 | 40226123 |
a0006 | 0/0 | 1050 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | MAAVK others(1045): Show |
chr15 | 40156069 | 40226123 |
a0007 | 0/0 | 1050 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | MAAVK others(1045): Show |
chr15 | 40156069 | 40226123 |
a0008 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | MAAVK others(1045): Show |
chr15 | 40156069 | 40226123 |
a0009 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | MAAVK others(1045): Show |
chr15 | 40156069 | 40226123 |
a0010 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | MAAVK others(1045): Show |
chr15 | 40156069 | 40226123 |
a0011 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | MAAMK others(1045): Show |
chr15 | 40156069 | 40226123 |
a0012 | 0/0 | 1050 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | MAAVK others(1045): Show |
chr15 | 40156069 | 40226123 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002 | 0/0 | 3150 | 73 | 1 | 15 | 39 | 5 | 13 | BUB1B_chr15_40156069_40226123 | BUB1B | ATGGC others(3145): Show |
chr15 | 40156069 | 40226123 | ||
a0001c0003 | 0/0 | 3150 | 67 | 12 | 7 | 38 | 2 | 8 | BUB1B_chr15_40156069_40226123 | BUB1B | ATGGC others(3145): Show |
chr15 | 40156069 | 40226123 | ||
a0001c0004 | 0/0 | 3150 | 33 | 20 | 6 | 0 | 3 | 4 | BUB1B_chr15_40156069_40226123 | BUB1B | ATGGC others(3145): Show |
chr15 | 40156069 | 40226123 | ||
a0001c0008 | 0/0 | 3150 | 2 | 0 | 0 | 2 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | ATGGC others(3145): Show |
chr15 | 40156069 | 40226123 | ||
a0001c0015 | 0/0 | 3150 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | ATGGC others(3145): Show |
chr15 | 40156069 | 40226123 | ||
a0001c0019 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | ATGGC others(3145): Show |
chr15 | 40156069 | 40226123 | ||
a0002c0001 | 1/1 | 3150 | 119 | 11 | 24 | 69 | 2 | 11 | BUB1B_chr15_40156069_40226123 | BUB1B | ATGGC others(3145): Show |
chr15 | 40156069 | 40226123 | ||
a0002c0013 | 0/0 | 3150 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | ATGGC others(3145): Show |
chr15 | 40156069 | 40226123 | ||
a0002c0016 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | ATGGC others(3145): Show |
chr15 | 40156069 | 40226123 | ||
a0003c0005 | 0/0 | 3150 | 27 | 26 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | ATGGC others(3145): Show |
chr15 | 40156069 | 40226123 | ||
a0003c0020 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | ATGGC others(3145): Show |
chr15 | 40156069 | 40226123 | ||
a0004c0006 | 0/0 | 3150 | 9 | 8 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | ATGGC others(3145): Show |
chr15 | 40156069 | 40226123 | ||
a0005c0007 | 0/0 | 3150 | 9 | 7 | 2 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | ATGGC others(3145): Show |
chr15 | 40156069 | 40226123 | ||
a0006c0009 | 0/0 | 3150 | 2 | 0 | 0 | 2 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | ATGGC others(3145): Show |
chr15 | 40156069 | 40226123 | ||
a0007c0014 | 0/0 | 3150 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | ATGGC others(3145): Show |
chr15 | 40156069 | 40226123 | ||
a0008c0011 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | ATGGC others(3145): Show |
chr15 | 40156069 | 40226123 | ||
a0009c0018 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | ATGGC others(3145): Show |
chr15 | 40156069 | 40226123 | ||
a0010c0012 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | ATGGC others(3145): Show |
chr15 | 40156069 | 40226123 | ||
a0011c0010 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | ATGGC others(3145): Show |
chr15 | 40156069 | 40226123 | ||
a0012c0017 | 0/0 | 3150 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | ATGGC others(3145): Show |
chr15 | 40156069 | 40226123 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001 | 0/0 | 3669 | 73 | 1 | 15 | 39 | 5 | 13 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0001c0003t0001 | 0/0 | 3669 | 66 | 12 | 7 | 37 | 2 | 8 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0001c0003t0006 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0001c0004t0001 | 0/0 | 3669 | 31 | 19 | 5 | 0 | 3 | 4 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0001c0004t0004 | 0/0 | 3669 | 2 | 1 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0001c0008t0001 | 0/0 | 3669 | 2 | 0 | 0 | 2 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0001c0015t0001 | 0/0 | 3669 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0001c0019t0003 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0002c0001t0001 | 0/0 | 3669 | 4 | 0 | 1 | 2 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0002c0001t0002 | 1/1 | 3669 | 114 | 11 | 23 | 66 | 2 | 10 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0002c0001t0005 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0002c0013t0002 | 0/0 | 3669 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0002c0016t0002 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0003c0005t0003 | 0/0 | 3669 | 27 | 26 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0003c0020t0003 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0004c0006t0001 | 0/0 | 3669 | 4 | 4 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0004c0006t0002 | 0/0 | 3669 | 5 | 4 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0005c0007t0003 | 0/0 | 3669 | 9 | 7 | 2 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0006c0009t0002 | 0/0 | 3669 | 2 | 0 | 0 | 2 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0007c0014t0001 | 0/0 | 3669 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0008c0011t0001 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0009c0018t0003 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0010c0012t0001 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0011c0010t0001 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
a0012c0017t0002 | 0/0 | 3669 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | GTGGG others(3664): Show |
chr15 | 40156069 | 40226123 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0002t0001g0001 | 0/0 | 11 | 0 | 3 | 7 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0007 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0003t0006g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0003 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0001g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0004g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0004t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0008t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0008t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0015t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0001c0019t0003g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0002 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0017 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0182 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0204 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0002g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0001t0005g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0013t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0002c0016t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0005t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0003c0020t0003g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0004c0006t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0004c0006t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0004c0006t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0004c0006t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0004c0006t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0004c0006t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0004c0006t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0004c0006t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0004c0006t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0005c0007t0003g0005 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0005c0007t0003g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0005c0007t0003g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0005c0007t0003g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0005c0007t0003g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0005c0007t0003g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0006c0009t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0006c0009t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0007c0014t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0008c0011t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0009c0018t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0010c0012t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0011c0010t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
a0012c0017t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0001 | g0089 | EUR | GBR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0162 | EUR | GBR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00140 | hp1 | a0001 | c0004 | t0001 | g0289 | EUR | GBR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00140 | hp2 | a0001 | c0003 | t0001 | g0071 | EUR | GBR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0007 | EUR | FIN | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00280 | hp2 | a0002 | c0001 | t0002 | g0017 | EUR | FIN | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | CHS | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00408 | hp2 | a0002 | c0001 | t0002 | g0218 | EAS | CHS | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00544 | hp1 | a0002 | c0001 | t0002 | g0019 | EAS | CHS | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00544 | hp2 | a0002 | c0001 | t0002 | g0023 | EAS | CHS | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00597 | hp1 | a0002 | c0001 | t0002 | g0251 | EAS | CHS | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00597 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | CHS | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | CHS | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00609 | hp2 | a0002 | c0001 | t0002 | g0181 | EAS | CHS | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00621 | hp1 | a0002 | c0001 | t0002 | g0273 | EAS | CHS | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00621 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | CHS | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00642 | hp1 | a0002 | c0001 | t0002 | g0018 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00642 | hp2 | a0003 | c0005 | t0003 | g0124 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0059 | EAS | CHS | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00673 | hp2 | a0002 | c0001 | t0002 | g0254 | EAS | CHS | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00733 | hp2 | a0002 | c0001 | t0002 | g0189 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00735 | hp1 | a0001 | c0004 | t0004 | g0298 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00735 | hp2 | a0001 | c0004 | t0001 | g0285 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00741 | hp1 | a0002 | c0001 | t0002 | g0217 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG00741 | hp2 | a0004 | c0006 | t0002 | g0157 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01069 | hp1 | a0001 | c0002 | t0001 | g0078 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01069 | hp2 | a0001 | c0003 | t0001 | g0087 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01081 | hp1 | a0005 | c0007 | t0003 | g0303 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01081 | hp2 | a0002 | c0001 | t0002 | g0198 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01106 | hp1 | a0002 | c0001 | t0002 | g0195 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01106 | hp2 | a0001 | c0004 | t0001 | g0290 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01109 | hp1 | a0001 | c0004 | t0001 | g0165 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01109 | hp2 | a0002 | c0001 | t0002 | g0259 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01167 | hp1 | a0002 | c0001 | t0002 | g0197 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01167 | hp2 | a0001 | c0003 | t0001 | g0028 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01168 | hp1 | a0001 | c0003 | t0001 | g0279 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01168 | hp2 | a0002 | c0001 | t0002 | g0184 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01169 | hp1 | a0001 | c0003 | t0001 | g0278 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01169 | hp2 | a0001 | c0003 | t0001 | g0086 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0163 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01175 | hp2 | a0002 | c0001 | t0002 | g0219 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01243 | hp1 | a0005 | c0007 | t0003 | g0304 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01243 | hp2 | a0002 | c0001 | t0002 | g0305 | AMR | PUR | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01255 | hp1 | a0001 | c0003 | t0001 | g0224 | AMR | CLM | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01255 | hp2 | a0002 | c0001 | t0002 | g0166 | AMR | CLM | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01257 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01257 | hp2 | a0002 | c0001 | t0001 | g0253 | AMR | CLM | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01258 | hp1 | a0001 | c0002 | t0001 | g0007 | AMR | CLM | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01258 | hp2 | a0002 | c0001 | t0002 | g0017 | AMR | CLM | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01361 | hp1 | a0002 | c0001 | t0002 | g0208 | AMR | CLM | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0099 | AMR | CLM | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01433 | hp1 | a0002 | c0001 | t0002 | g0187 | AMR | CLM | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01433 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | CLM | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | CLM | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01496 | hp2 | a0002 | c0001 | t0002 | g0180 | AMR | CLM | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01516 | hp1 | a0001 | c0002 | t0001 | g0040 | EUR | IBS | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01516 | hp2 | a0001 | c0004 | t0001 | g0281 | EUR | IBS | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01517 | hp1 | a0001 | c0004 | t0001 | g0288 | EUR | IBS | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01517 | hp2 | a0001 | c0002 | t0001 | g0050 | EUR | IBS | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01884 | hp1 | a0001 | c0004 | t0001 | g0293 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01884 | hp2 | a0002 | c0001 | t0002 | g0190 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01891 | hp1 | a0005 | c0007 | t0003 | g0300 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01891 | hp2 | a0002 | c0001 | t0002 | g0177 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01952 | hp1 | a0002 | c0001 | t0002 | g0022 | AMR | PEL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0064 | AMR | PEL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01975 | hp1 | a0001 | c0004 | t0001 | g0284 | AMR | PEL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01978 | hp1 | a0002 | c0001 | t0002 | g0176 | AMR | PEL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01978 | hp2 | a0001 | c0002 | t0001 | g0041 | AMR | PEL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02004 | hp1 | a0001 | c0002 | t0001 | g0048 | AMR | PEL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02004 | hp2 | a0002 | c0001 | t0002 | g0255 | AMR | PEL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02027 | hp1 | a0007 | c0014 | t0001 | g0096 | EAS | KHV | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02027 | hp2 | a0002 | c0001 | t0002 | g0212 | EAS | KHV | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02040 | hp1 | a0002 | c0001 | t0002 | g0186 | EAS | KHV | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02040 | hp2 | a0001 | c0002 | t0001 | g0060 | EAS | KHV | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02055 | hp1 | a0003 | c0005 | t0003 | g0116 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02055 | hp2 | a0003 | c0005 | t0003 | g0122 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02071 | hp1 | a0006 | c0009 | t0002 | g0002 | EAS | KHV | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0062 | EAS | KHV | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02074 | hp1 | a0002 | c0001 | t0002 | g0240 | EAS | KHV | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | KHV | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02083 | hp1 | a0002 | c0001 | t0002 | g0183 | EAS | KHV | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02083 | hp2 | a0001 | c0002 | t0001 | g0100 | EAS | KHV | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02129 | hp1 | a0002 | c0001 | t0002 | g0172 | EAS | KHV | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02129 | hp2 | a0001 | c0003 | t0001 | g0021 | EAS | KHV | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0052 | EAS | KHV | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02132 | hp2 | a0002 | c0001 | t0002 | g0248 | EAS | KHV | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02145 | hp1 | a0001 | c0003 | t0001 | g0150 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02145 | hp2 | a0003 | c0005 | t0003 | g0146 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02148 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02148 | hp2 | a0002 | c0001 | t0002 | g0260 | AMR | PEL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02155 | hp1 | a0002 | c0001 | t0002 | g0257 | EAS | CDX | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0057 | EAS | CDX | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02165 | hp1 | a0002 | c0001 | t0002 | g0264 | EAS | CDX | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02165 | hp2 | a0001 | c0003 | t0001 | g0232 | EAS | CDX | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02257 | hp1 | a0005 | c0007 | t0003 | g0301 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02257 | hp2 | a0001 | c0004 | t0001 | g0003 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02258 | hp1 | a0004 | c0006 | t0002 | g0153 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02258 | hp2 | a0003 | c0005 | t0003 | g0126 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02273 | hp1 | a0002 | c0001 | t0002 | g0022 | AMR | PEL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02273 | hp2 | a0001 | c0002 | t0001 | g0055 | AMR | PEL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02280 | hp1 | a0003 | c0005 | t0003 | g0016 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02280 | hp2 | a0005 | c0007 | t0003 | g0005 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02293 | hp1 | a0001 | c0002 | t0001 | g0046 | AMR | PEL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02293 | hp2 | a0002 | c0001 | t0002 | g0294 | AMR | PEL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02300 | hp1 | a0001 | c0004 | t0001 | g0291 | AMR | PEL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02300 | hp2 | a0002 | c0001 | t0002 | g0209 | AMR | PEL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02451 | hp1 | a0004 | c0006 | t0002 | g0155 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02451 | hp2 | a0008 | c0011 | t0001 | g0276 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02523 | hp1 | a0002 | c0001 | t0002 | g0261 | EAS | KHV | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02523 | hp2 | a0001 | c0003 | t0001 | g0012 | EAS | KHV | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02572 | hp1 | a0001 | c0004 | t0001 | g0130 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02572 | hp2 | a0001 | c0004 | t0001 | g0282 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02602 | hp1 | a0002 | c0001 | t0002 | g0207 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0051 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02615 | hp1 | a0004 | c0006 | t0001 | g0032 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02615 | hp2 | a0005 | c0007 | t0003 | g0005 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02622 | hp1 | a0009 | c0018 | t0003 | g0142 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02622 | hp2 | a0002 | c0001 | t0002 | g0193 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0226 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02630 | hp2 | a0001 | c0004 | t0001 | g0136 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02647 | hp1 | a0003 | c0020 | t0003 | g0112 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02647 | hp2 | a0004 | c0006 | t0002 | g0154 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02717 | hp1 | a0003 | c0005 | t0003 | g0140 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0152 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02723 | hp1 | a0002 | c0001 | t0002 | g0138 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02723 | hp2 | a0005 | c0007 | t0003 | g0005 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02735 | hp1 | a0002 | c0001 | t0002 | g0272 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02735 | hp2 | a0001 | c0002 | t0001 | g0037 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02809 | hp1 | a0002 | c0001 | t0002 | g0173 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02809 | hp2 | a0001 | c0003 | t0001 | g0228 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02818 | hp1 | a0001 | c0003 | t0001 | g0085 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02818 | hp2 | a0001 | c0019 | t0003 | g0143 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02886 | hp1 | a0001 | c0003 | t0001 | g0149 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02886 | hp2 | a0010 | c0012 | t0001 | g0280 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02895 | hp1 | a0003 | c0005 | t0003 | g0113 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02895 | hp2 | a0001 | c0004 | t0001 | g0129 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02896 | hp1 | a0001 | c0004 | t0001 | g0133 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02896 | hp2 | a0003 | c0005 | t0003 | g0125 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02922 | hp1 | a0001 | c0004 | t0001 | g0134 | AFR | ESN | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02922 | hp2 | a0001 | c0003 | t0001 | g0151 | AFR | ESN | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0075 | AFR | ESN | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02965 | hp2 | a0003 | c0005 | t0003 | g0120 | AFR | ESN | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02976 | hp1 | a0001 | c0003 | t0001 | g0227 | AFR | ESN | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02976 | hp2 | a0003 | c0005 | t0003 | g0118 | AFR | ESN | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03017 | hp1 | a0001 | c0003 | t0001 | g0081 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03017 | hp2 | a0002 | c0001 | t0002 | g0222 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03041 | hp1 | a0003 | c0005 | t0003 | g0123 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03041 | hp2 | a0011 | c0010 | t0001 | g0277 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03098 | hp1 | a0002 | c0001 | t0002 | g0178 | AFR | MSL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03098 | hp2 | a0004 | c0006 | t0001 | g0034 | AFR | MSL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03130 | hp1 | a0003 | c0005 | t0003 | g0117 | AFR | ESN | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03130 | hp2 | a0003 | c0005 | t0003 | g0121 | AFR | ESN | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03139 | hp1 | a0002 | c0001 | t0002 | g0191 | AFR | ESN | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03139 | hp2 | a0001 | c0004 | t0001 | g0003 | AFR | ESN | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03195 | hp1 | a0003 | c0005 | t0003 | g0139 | AFR | ESN | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03195 | hp2 | a0001 | c0004 | t0001 | g0003 | AFR | ESN | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03209 | hp1 | a0003 | c0005 | t0003 | g0114 | AFR | MSL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03209 | hp2 | a0002 | c0001 | t0002 | g0192 | AFR | MSL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03225 | hp1 | a0001 | c0004 | t0001 | g0132 | AFR | MSL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03225 | hp2 | a0012 | c0017 | t0002 | g0174 | AFR | MSL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03239 | hp1 | a0001 | c0003 | t0001 | g0027 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03239 | hp2 | a0001 | c0003 | t0001 | g0095 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03453 | hp1 | a0003 | c0005 | t0003 | g0115 | AFR | MSL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03453 | hp2 | a0001 | c0004 | t0001 | g0003 | AFR | MSL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03486 | hp1 | a0001 | c0004 | t0001 | g0003 | AFR | MSL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03486 | hp2 | a0003 | c0005 | t0003 | g0008 | AFR | MSL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03490 | hp1 | a0001 | c0004 | t0001 | g0283 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03490 | hp2 | a0001 | c0002 | t0001 | g0107 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03491 | hp1 | a0001 | c0002 | t0001 | g0036 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0058 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03492 | hp1 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03492 | hp2 | a0001 | c0004 | t0001 | g0287 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03540 | hp1 | a0001 | c0004 | t0001 | g0024 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03540 | hp2 | a0001 | c0004 | t0001 | g0131 | AFR | GWD | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03579 | hp1 | a0001 | c0004 | t0001 | g0024 | AFR | MSL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03579 | hp2 | a0003 | c0005 | t0003 | g0145 | AFR | MSL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03654 | hp1 | a0001 | c0015 | t0001 | g0090 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03654 | hp2 | a0001 | c0004 | t0001 | g0286 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03669 | hp1 | a0002 | c0001 | t0002 | g0201 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03669 | hp2 | a0001 | c0003 | t0001 | g0082 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03688 | hp1 | a0002 | c0001 | t0002 | g0203 | SAS | STU | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0073 | SAS | STU | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03704 | hp1 | a0001 | c0002 | t0001 | g0074 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03704 | hp2 | a0001 | c0002 | t0001 | g0047 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03710 | hp1 | a0002 | c0001 | t0002 | g0295 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03710 | hp2 | a0002 | c0001 | t0002 | g0019 | SAS | PJL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03831 | hp1 | a0001 | c0002 | t0001 | g0072 | SAS | BEB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03831 | hp2 | a0001 | c0003 | t0001 | g0045 | SAS | BEB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03927 | hp1 | a0002 | c0001 | t0002 | g0210 | SAS | BEB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0001 | SAS | BEB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03942 | hp1 | a0001 | c0004 | t0001 | g0236 | SAS | BEB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03942 | hp2 | a0001 | c0003 | t0001 | g0234 | SAS | BEB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG04115 | hp1 | a0002 | c0013 | t0002 | g0205 | SAS | STU | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG04115 | hp2 | a0001 | c0003 | t0001 | g0109 | SAS | STU | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0093 | SAS | BEB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG04184 | hp2 | a0002 | c0001 | t0001 | g0164 | SAS | BEB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG04199 | hp1 | a0002 | c0001 | t0002 | g0196 | SAS | STU | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG04199 | hp2 | a0001 | c0003 | t0001 | g0083 | SAS | STU | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0076 | SAS | STU | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG04204 | hp2 | a0002 | c0001 | t0002 | g0246 | SAS | STU | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18522 | hp1 | a0003 | c0005 | t0003 | g0144 | AFR | YRI | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18522 | hp2 | a0001 | c0004 | t0001 | g0135 | AFR | YRI | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18747 | hp1 | a0001 | c0003 | t0001 | g0070 | EAS | CHB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18747 | hp2 | a0002 | c0001 | t0002 | g0245 | EAS | CHB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18906 | hp1 | a0002 | c0001 | t0002 | g0194 | AFR | YRI | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18906 | hp2 | a0004 | c0006 | t0001 | g0031 | AFR | YRI | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18939 | hp1 | a0001 | c0003 | t0001 | g0021 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18939 | hp2 | a0001 | c0003 | t0001 | g0106 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18940 | hp1 | a0001 | c0003 | t0001 | g0158 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18940 | hp2 | a0002 | c0001 | t0002 | g0220 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18944 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18944 | hp2 | a0002 | c0001 | t0002 | g0188 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18945 | hp1 | a0001 | c0003 | t0001 | g0084 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18945 | hp2 | a0002 | c0001 | t0002 | g0171 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18946 | hp1 | a0001 | c0003 | t0001 | g0069 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18946 | hp2 | a0002 | c0001 | t0002 | g0237 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18947 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18947 | hp2 | a0002 | c0001 | t0002 | g0213 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18949 | hp2 | a0002 | c0016 | t0002 | g0252 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18950 | hp1 | a0002 | c0001 | t0002 | g0242 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18950 | hp2 | a0001 | c0003 | t0001 | g0168 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18952 | hp1 | a0002 | c0001 | t0002 | g0002 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18952 | hp2 | a0001 | c0003 | t0001 | g0103 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18953 | hp1 | a0002 | c0001 | t0002 | g0238 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18953 | hp2 | a0002 | c0001 | t0001 | g0101 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18954 | hp1 | a0006 | c0009 | t0002 | g0179 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18954 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18957 | hp1 | a0002 | c0001 | t0002 | g0266 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18957 | hp2 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18959 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18959 | hp2 | a0002 | c0001 | t0002 | g0167 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18960 | hp1 | a0002 | c0001 | t0002 | g0267 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18962 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18962 | hp2 | a0002 | c0001 | t0002 | g0256 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18964 | hp1 | a0002 | c0001 | t0002 | g0214 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18964 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18965 | hp1 | a0001 | c0003 | t0001 | g0079 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18965 | hp2 | a0001 | c0003 | t0001 | g0231 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18966 | hp1 | a0001 | c0002 | t0001 | g0011 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18966 | hp2 | a0002 | c0001 | t0002 | g0268 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0054 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18970 | hp2 | a0002 | c0001 | t0002 | g0002 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18974 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18974 | hp2 | a0002 | c0001 | t0002 | g0270 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18977 | hp1 | a0002 | c0001 | t0002 | g0200 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18977 | hp2 | a0002 | c0001 | t0002 | g0258 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18979 | hp1 | a0001 | c0008 | t0001 | g0105 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18979 | hp2 | a0002 | c0001 | t0002 | g0239 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18981 | hp1 | a0002 | c0001 | t0002 | g0297 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18981 | hp2 | a0001 | c0003 | t0001 | g0108 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18982 | hp1 | a0001 | c0003 | t0001 | g0104 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0091 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18983 | hp1 | a0002 | c0001 | t0002 | g0250 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18983 | hp2 | a0001 | c0003 | t0001 | g0159 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18984 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18984 | hp2 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18986 | hp1 | a0001 | c0003 | t0001 | g0229 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18986 | hp2 | a0002 | c0001 | t0002 | g0243 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18987 | hp1 | a0001 | c0003 | t0001 | g0012 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18987 | hp2 | a0002 | c0001 | t0002 | g0247 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18988 | hp1 | a0002 | c0001 | t0002 | g0296 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18988 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18989 | hp1 | a0002 | c0001 | t0002 | g0223 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18989 | hp2 | a0001 | c0003 | t0001 | g0097 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18990 | hp1 | a0002 | c0001 | t0002 | g0199 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0044 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18992 | hp1 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18992 | hp2 | a0002 | c0001 | t0002 | g0269 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18993 | hp1 | a0002 | c0001 | t0002 | g0221 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18993 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18997 | hp1 | a0001 | c0003 | t0001 | g0235 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA18997 | hp2 | a0001 | c0002 | t0001 | g0042 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19001 | hp2 | a0002 | c0001 | t0002 | g0263 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19003 | hp1 | a0002 | c0001 | t0002 | g0002 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19003 | hp2 | a0001 | c0003 | t0001 | g0038 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19005 | hp1 | a0002 | c0001 | t0002 | g0216 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19005 | hp2 | a0001 | c0003 | t0001 | g0015 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19006 | hp1 | a0002 | c0001 | t0002 | g0020 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19006 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19007 | hp1 | a0001 | c0003 | t0001 | g0009 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19007 | hp2 | a0002 | c0001 | t0002 | g0241 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19009 | hp1 | a0002 | c0001 | t0002 | g0262 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0098 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19011 | hp1 | a0002 | c0001 | t0001 | g0102 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19011 | hp2 | a0001 | c0003 | t0001 | g0161 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19030 | hp1 | a0001 | c0004 | t0001 | g0137 | AFR | LWK | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19030 | hp2 | a0003 | c0005 | t0003 | g0141 | AFR | LWK | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19043 | hp1 | a0005 | c0007 | t0003 | g0302 | AFR | LWK | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0025 | AFR | LWK | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19054 | hp1 | a0002 | c0001 | t0002 | g0023 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19054 | hp2 | a0001 | c0008 | t0001 | g0080 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19057 | hp1 | a0001 | c0003 | t0001 | g0039 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19057 | hp2 | a0002 | c0001 | t0002 | g0202 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19058 | hp1 | a0002 | c0001 | t0002 | g0169 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19058 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19060 | hp1 | a0001 | c0003 | t0001 | g0233 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19062 | hp1 | a0002 | c0001 | t0002 | g0274 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19065 | hp2 | a0002 | c0001 | t0002 | g0170 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19066 | hp2 | a0002 | c0001 | t0002 | g0020 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19068 | hp2 | a0002 | c0001 | t0002 | g0206 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19070 | hp1 | a0002 | c0001 | t0002 | g0002 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19070 | hp2 | a0001 | c0003 | t0001 | g0014 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19074 | hp1 | a0002 | c0001 | t0002 | g0111 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19074 | hp2 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19078 | hp1 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19078 | hp2 | a0002 | c0001 | t0002 | g0249 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19079 | hp1 | a0001 | c0003 | t0001 | g0004 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19079 | hp2 | a0002 | c0001 | t0005 | g0275 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19080 | hp2 | a0002 | c0001 | t0002 | g0002 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19081 | hp2 | a0002 | c0001 | t0002 | g0215 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19083 | hp1 | a0002 | c0001 | t0002 | g0175 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19083 | hp2 | a0001 | c0002 | t0001 | g0092 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19084 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19084 | hp2 | a0001 | c0003 | t0001 | g0230 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19088 | hp1 | a0002 | c0001 | t0002 | g0244 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19088 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19089 | hp1 | a0001 | c0003 | t0006 | g0160 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19089 | hp2 | a0002 | c0001 | t0002 | g0185 | EAS | JPT | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19240 | hp1 | a0003 | c0005 | t0003 | g0008 | AFR | YRI | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA19240 | hp2 | a0004 | c0006 | t0001 | g0033 | AFR | YRI | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA20129 | hp1 | a0003 | c0005 | t0003 | g0119 | AFR | ASW | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA20129 | hp2 | a0002 | c0001 | t0002 | g0265 | AFR | ASW | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0053 | EUR | TSI | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA20805 | hp2 | a0002 | c0001 | t0002 | g0018 | EUR | TSI | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01123 | hp1 | a0001 | c0003 | t0001 | g0088 | AMR | CLM | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG01123 | hp2 | a0002 | c0001 | t0002 | g0271 | AMR | CLM | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02109 | hp1 | a0005 | c0007 | t0003 | g0005 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02109 | hp2 | a0003 | c0005 | t0003 | g0128 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02486 | hp1 | a0001 | c0004 | t0004 | g0299 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02486 | hp2 | a0001 | c0003 | t0001 | g0225 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02559 | hp1 | a0001 | c0004 | t0001 | g0292 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG02559 | hp2 | a0001 | c0003 | t0001 | g0147 | AFR | ACB | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03471 | hp1 | a0001 | c0003 | t0001 | g0148 | AFR | MSL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG03471 | hp2 | a0003 | c0005 | t0003 | g0127 | AFR | MSL | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG06807 | hp1 | a0004 | c0006 | t0002 | g0156 | AFR | USA | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
HG06807 | hp2 | a0003 | c0005 | t0003 | g0008 | AFR | USA | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA21309 | hp1 | a0002 | c0001 | t0002 | g0211 | AFR | LWK | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
NA21309 | hp2 | a0003 | c0005 | t0003 | g0016 | AFR | LWK | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
homoSapiens | chm13v2 | a0002 | c0001 | t0002 | g0182 | REF | REF | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
homoSapiens | grch38p0 | a0002 | c0001 | t0002 | g0204 | REF | REF | BUB1B_chr15_40156069_40226123 | BUB1B | chr15 | 40156069 | 40226123 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:40161230 | G | A | 1 | a0011 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.10G>A | p.Val4Met | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/23 | 162/3669 | 10/3153 | 4/1050 | chr15 | 40161230 | |||
chr15:40165136 | C | T | 1 | a0005 | 9 | HG01081.hp1 HG01243.hp1 HG01891.hp1 others(6): Show |
missense_variant | MODERATE | c.119C>T | p.Thr40Met | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/23 | 271/3669 | 119/3153 | 40/1050 | chr15 | 40165136 | |||
chr15:40170479 | A | AAGAACAA others(57): Show |
1 | a0001 | 1 | HG03490.hp2 | frameshift_variant&stop_gained | HIGH | c.240-55_248dupAACAA others(59): Show |
p.Ser83fs | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/23 | 401/3669 | 249/3153 | 83/1050 | INFO_REALIGN_3_PRIME | chr15 | 40170479 | ||
chr15:40185218 | A | G | 1 | a0010 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.805A>G | p.Asn269Asp | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 7/23 | 957/3669 | 805/3153 | 269/1050 | chr15 | 40185218 | |||
chr15:40185587 | G | C | 1 | a0009 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.1003G>C | p.Ala335Pro | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/23 | 1155/3669 | 1003/3153 | 335/1050 | chr15 | 40185587 | |||
chr15:40185630 | G | A | 9 | a0001 a0003 a0004 others(6): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
missense_variant | MODERATE | c.1046G>A | p.Arg349Gln | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/23 | 1198/3669 | 1046/3153 | 349/1050 | chr15 | 40185630 | |||
chr15:40196656 | G | C | 1 | a0004 | 9 | HG00741.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
missense_variant | MODERATE | c.1170G>C | p.Glu390Asp | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 9/23 | 1322/3669 | 1170/3153 | 390/1050 | chr15 | 40196656 | |||
chr15:40196747 | C | T | 1 | a0012 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.1261C>T | p.Arg421Trp | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 9/23 | 1413/3669 | 1261/3153 | 421/1050 | chr15 | 40196747 | |||
chr15:40202609 | G | A | 1 | a0006 | 2 | HG02071.hp1 NA18954.hp1 |
missense_variant | MODERATE | c.1649G>A | p.Arg550Gln | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/23 | 1801/3669 | 1649/3153 | 550/1050 | chr15 | 40202609 | |||
chr15:40206302 | T | C | 3 | a0003 a0005 a0009 |
38 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(35): Show |
missense_variant | MODERATE | c.1853T>C | p.Val618Ala | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 15/23 | 2005/3669 | 1853/3153 | 618/1050 | chr15 | 40206302 | |||
chr15:40206324 | A | G | 1 | a0007 | 1 | HG02027.hp1 | missense_variant | MODERATE | c.1875A>G | p.Ile625Met | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 15/23 | 2027/3669 | 1875/3153 | 625/1050 | chr15 | 40206324 | |||
chr15:40220617 | A | G | 2 | a0008 a0011 |
2 | HG02451.hp2 HG03041.hp2 |
missense_variant | MODERATE | c.3011A>G | p.Asn1004Ser | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 23/23 | 3163/3669 | 3011/3153 | 1004/1050 | chr15 | 40220617 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:40161229 | G | T | 4 | a0001c0019 a0003c0005 a0003c0020 others(1): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
synonymous_variant | LOW | c.9G>T | p.Ala3Ala | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/23 | 161/3669 | 9/3153 | 3/1050 | chr15 | 40161229 | |||
chr15:40170579 | G | A | 4 | a0001c0004 a0008c0011 a0010c0012 others(1): Show |
36 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(33): Show |
synonymous_variant | LOW | c.282G>A | p.Lys94Lys | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/23 | 434/3669 | 282/3153 | 94/1050 | chr15 | 40170579 | |||
chr15:40183810 | A | G | 1 | a0003c0020 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.678A>G | p.Thr226Thr | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 6/23 | 830/3669 | 678/3153 | 226/1050 | chr15 | 40183810 | |||
chr15:40185319 | G | A | 1 | a0002c0013 | 1 | HG04115.hp1 | synonymous_variant | LOW | c.906G>A | p.Arg302Arg | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 7/23 | 1058/3669 | 906/3153 | 302/1050 | chr15 | 40185319 | |||
chr15:40196650 | G | A | 2 | a0001c0002 a0007c0014 |
74 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(71): Show |
synonymous_variant | LOW | c.1164G>A | p.Ala388Ala | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 9/23 | 1316/3669 | 1164/3153 | 388/1050 | chr15 | 40196650 | |||
chr15:40196716 | C | T | 1 | a0008c0011 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.1230C>T | p.Phe410Phe | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 9/23 | 1382/3669 | 1230/3153 | 410/1050 | chr15 | 40196716 | |||
chr15:40202460 | T | C | 1 | a0005c0007 | 9 | HG01081.hp1 HG01243.hp1 HG01891.hp1 others(6): Show |
synonymous_variant | LOW | c.1623T>C | p.Asn541Asn | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 13/23 | 1775/3669 | 1623/3153 | 541/1050 | chr15 | 40202460 | |||
chr15:40212594 | A | G | 1 | a0002c0016 | 1 | NA18949.hp2 | synonymous_variant | LOW | c.2481A>G | p.Gln827Gln | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 19/23 | 2633/3669 | 2481/3153 | 827/1050 | chr15 | 40212594 | |||
chr15:40212636 | C | T | 1 | a0005c0007 | 9 | HG01081.hp1 HG01243.hp1 HG01891.hp1 others(6): Show |
synonymous_variant | LOW | c.2523C>T | p.Cys841Cys | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 19/23 | 2675/3669 | 2523/3153 | 841/1050 | chr15 | 40212636 | |||
chr15:40217601 | C | T | 1 | a0001c0008 | 2 | NA18979.hp1 NA19054.hp2 |
synonymous_variant | LOW | c.2784C>T | p.Ser928Ser | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 21/23 | 2936/3669 | 2784/3153 | 928/1050 | chr15 | 40217601 | |||
chr15:40218461 | C | T | 1 | a0001c0015 | 1 | HG03654.hp1 | synonymous_variant | LOW | c.2856C>T | p.Asp952Asp | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 22/23 | 3008/3669 | 2856/3153 | 952/1050 | chr15 | 40218461 | |||
chr15:40220705 | A | G | 5 | a0001c0019 a0003c0005 a0003c0020 others(2): Show |
39 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(36): Show |
synonymous_variant | LOW | c.3099A>G | p.Lys1033Lys | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 23/23 | 3251/3669 | 3099/3153 | 1033/1050 | chr15 | 40220705 | |||
chr15:40220753 | T | C | 1 | a0008c0011 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.3147T>C | p.Phe1049Phe | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 23/23 | 3299/3669 | 3147/3153 | 1049/1050 | chr15 | 40220753 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:40161106 | A | G | 18 | a0001c0002t0001 a0001c0003t0001 a0001c0003t0006 others(15): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
5_prime_UTR_variant | MODIFIER | c.-115A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/23 | 115 | chr15 | 40161106 | ||||||
chr15:40161136 | G | A | 1 | a0002c0001t0005 | 1 | NA19079.hp2 | 5_prime_UTR_variant | MODIFIER | c.-85G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/23 | 85 | chr15 | 40161136 | ||||||
chr15:40161179 | A | G | 1 | a0001c0004t0004 | 2 | HG00735.hp1 HG02486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-42A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/23 | 42 | chr15 | 40161179 | ||||||
chr15:40220870 | A | G | 5 | a0001c0019t0003 a0003c0005t0003 a0003c0020t0003 others(2): Show |
39 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*111A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 23/23 | 111 | chr15 | 40220870 | ||||||
chr15:40220943 | A | G | 1 | a0001c0003t0006 | 1 | NA19089.hp1 | 3_prime_UTR_variant | MODIFIER | c.*184A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 23/23 | 184 | chr15 | 40220943 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:40161296 | G | A | 97 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(94): Show |
121 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.35+41G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40161296 | |||||||
chr15:40161312 | T | C | 1 | a0002c0001t0002g0111 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.35+57T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40161312 | |||||||
chr15:40162080 | G | A | 1 | a0003c0020t0003g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.35+825G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40162080 | |||||||
chr15:40162371 | G | C | 18 | a0003c0005t0003g0008 a0003c0005t0003g0113 a0003c0005t0003g0114 others(15): Show |
20 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.35+1116G>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40162371 | |||||||
chr15:40162720 | G | A | 10 | a0001c0004t0001g0003 a0001c0004t0001g0129 a0001c0004t0001g0130 others(7): Show |
14 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.35+1465G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40162720 | |||||||
chr15:40162860 | C | T | 1 | a0002c0001t0002g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.35+1605C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40162860 | |||||||
chr15:40162919 | C | T | 6 | a0005c0007t0003g0005 a0005c0007t0003g0300 a0005c0007t0003g0301 others(3): Show |
9 | HG01081.hp1 HG01243.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.35+1664C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40162919 | |||||||
chr15:40162926 | T | C | 1 | a0002c0001t0002g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.35+1671T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40162926 | |||||||
chr15:40162950 | G | A | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.35+1695G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40162950 | |||||||
chr15:40163182 | C | G | 2 | a0001c0004t0004g0298 a0001c0004t0004g0299 |
2 | HG00735.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.36-1871C>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40163182 | |||||||
chr15:40163434 | A | G | 1 | a0002c0001t0002g0297 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.36-1619A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40163434 | |||||||
chr15:40163446 | T | C | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.36-1607T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40163446 | |||||||
chr15:40163452 | C | T | 1 | a0002c0001t0002g0296 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.36-1601C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40163452 | |||||||
chr15:40163620 | C | T | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.36-1433C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40163620 | |||||||
chr15:40163693 | T | G | 121 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(118): Show |
148 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(145): Show |
intron_variant | MODIFIER | c.36-1360T>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40163693 | |||||||
chr15:40163874 | A | G | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.36-1179A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40163874 | |||||||
chr15:40163885 | A | G | 1 | a0002c0001t0002g0295 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.36-1168A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40163885 | |||||||
chr15:40163923 | C | G | 1 | a0002c0001t0002g0294 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.36-1130C>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40163923 | |||||||
chr15:40163945 | T | C | 1 | a0001c0003t0001g0025 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.36-1108T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40163945 | |||||||
chr15:40164036 | G | A | 1 | a0003c0005t0003g0113 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.36-1017G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40164036 | |||||||
chr15:40164131 | T | A | 4 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0001g0149 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.36-922T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40164131 | |||||||
chr15:40164181 | G | A | 11 | a0001c0004t0001g0003 a0001c0004t0001g0129 a0001c0004t0001g0130 others(8): Show |
15 | HG01109.hp1 HG02257.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.36-872G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40164181 | |||||||
chr15:40164262 | T | G | 23 | a0003c0005t0003g0008 a0003c0005t0003g0016 a0003c0005t0003g0113 others(20): Show |
26 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(23): Show |
intron_variant | MODIFIER | c.36-791T>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40164262 | |||||||
chr15:40164315 | A | AC | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.36-734dupC | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr15 | 40164315 | ||||||
chr15:40164372 | C | T | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.36-681C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40164372 | |||||||
chr15:40164662 | C | CT | 33 | a0001c0002t0001g0110 a0001c0003t0001g0278 a0001c0003t0001g0279 others(30): Show |
38 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.36-374dupT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr15 | 40164662 | ||||||
chr15:40164662 | CT | C | 8 | a0001c0002t0001g0006 a0001c0002t0001g0026 a0001c0002t0001g0029 others(5): Show |
10 | HG01167.hp2 HG01255.hp2 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.36-374delT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr15 | 40164662 | ||||||
chr15:40164702 | T | C | 1 | a0001c0003t0001g0168 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.36-351T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40164702 | |||||||
chr15:40164841 | A | C | 47 | a0002c0001t0001g0164 a0002c0001t0001g0253 a0002c0001t0002g0022 others(44): Show |
49 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.36-212A>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40164841 | |||||||
chr15:40164928 | A | C | 195 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(192): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.36-125A>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | chr15 | 40164928 | |||||||
chr15:40165037 | G | GT | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.36-13dupT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr15 | 40165037 | ||||||
chr15:40165230 | A | C | 18 | a0001c0004t0001g0024 a0001c0004t0001g0236 a0001c0004t0001g0281 others(15): Show |
19 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.179+34A>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40165230 | |||||||
chr15:40165434 | C | T | 95 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(92): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.179+238C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40165434 | |||||||
chr15:40165477 | A | G | 1 | a0002c0001t0005g0275 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.179+281A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40165477 | |||||||
chr15:40165851 | A | AT | 44 | a0001c0003t0001g0025 a0001c0003t0001g0109 a0001c0004t0001g0024 others(41): Show |
47 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.179+671dupT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr15 | 40165851 | ||||||
chr15:40165851 | A | ATT | 5 | a0003c0005t0003g0016 a0003c0005t0003g0139 a0003c0005t0003g0140 others(2): Show |
6 | HG02280.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.179+670_179+671dup others(2): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr15 | 40165851 | ||||||
chr15:40165943 | C | T | 1 | a0002c0001t0002g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.179+747C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40165943 | |||||||
chr15:40165946 | G | A | 2 | a0001c0002t0001g0035 a0001c0002t0001g0036 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.179+750G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40165946 | |||||||
chr15:40165957 | AT | A | 31 | a0001c0004t0001g0003 a0001c0004t0001g0024 a0001c0004t0001g0129 others(28): Show |
36 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.179+763delT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr15 | 40165957 | ||||||
chr15:40165968 | T | C | 4 | a0003c0005t0003g0114 a0003c0005t0003g0115 a0003c0005t0003g0116 others(1): Show |
4 | HG02055.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.179+772T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40165968 | |||||||
chr15:40165997 | C | T | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.179+801C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40165997 | |||||||
chr15:40166339 | C | CT | 11 | a0001c0003t0001g0021 a0001c0003t0001g0168 a0001c0003t0001g0229 others(8): Show |
12 | HG01168.hp1 HG01169.hp1 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.179+1155dupT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr15 | 40166339 | ||||||
chr15:40166544 | G | A | 1 | a0001c0002t0001g0037 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.179+1348G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40166544 | |||||||
chr15:40166606 | C | T | 116 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(113): Show |
143 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.179+1410C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40166606 | |||||||
chr15:40166864 | C | T | 1 | a0002c0001t0002g0274 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.179+1668C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40166864 | |||||||
chr15:40166892 | C | A | 3 | a0001c0003t0001g0004 a0001c0003t0001g0009 a0001c0003t0001g0038 |
7 | NA18964.hp2 NA18984.hp1 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.179+1696C>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40166892 | |||||||
chr15:40167179 | T | G | 4 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0001g0149 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.179+1983T>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40167179 | |||||||
chr15:40167218 | A | G | 4 | a0001c0003t0001g0158 a0001c0003t0001g0159 a0001c0003t0001g0161 others(1): Show |
4 | NA18940.hp1 NA18983.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.179+2022A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40167218 | |||||||
chr15:40167264 | T | C | 1 | a0001c0004t0001g0165 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.179+2068T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40167264 | |||||||
chr15:40167271 | C | T | 1 | a0001c0002t0001g0030 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.179+2075C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40167271 | |||||||
chr15:40167342 | C | CT | 53 | a0001c0002t0001g0029 a0001c0002t0001g0098 a0001c0002t0001g0099 others(50): Show |
58 | HG00408.hp2 HG00621.hp1 HG00642.hp2 others(55): Show |
intron_variant | MODIFIER | c.179+2171dupT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr15 | 40167342 | ||||||
chr15:40167342 | C | CTT | 9 | a0001c0003t0001g0108 a0001c0003t0001g0149 a0001c0003t0001g0150 others(6): Show |
12 | HG01081.hp1 HG01243.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.179+2170_179+2171d others(4): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr15 | 40167342 | ||||||
chr15:40167342 | CT | C | 7 | a0001c0003t0001g0039 a0001c0003t0001g0278 a0002c0001t0002g0169 others(4): Show |
7 | HG01169.hp1 NA18946.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.179+2171delT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr15 | 40167342 | ||||||
chr15:40167428 | C | T | 1 | a0001c0004t0001g0293 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.179+2232C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40167428 | |||||||
chr15:40167503 | T | C | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.179+2307T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40167503 | |||||||
chr15:40167507 | T | C | 1 | a0010c0012t0001g0280 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.179+2311T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40167507 | |||||||
chr15:40167508 | A | G | 1 | a0001c0003t0001g0095 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.179+2312A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40167508 | |||||||
chr15:40167583 | C | T | 2 | a0001c0003t0001g0147 a0001c0003t0001g0148 |
2 | HG02559.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.179+2387C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40167583 | |||||||
chr15:40167596 | C | T | 18 | a0001c0004t0001g0024 a0001c0004t0001g0236 a0001c0004t0001g0281 others(15): Show |
19 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.179+2400C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40167596 | |||||||
chr15:40167637 | A | T | 1 | a0004c0006t0001g0034 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.180-2425A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40167637 | |||||||
chr15:40167778 | A | AT | 105 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(102): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.180-2273dupT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr15 | 40167778 | ||||||
chr15:40168024 | G | T | 196 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(193): Show |
232 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(229): Show |
intron_variant | MODIFIER | c.180-2038G>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40168024 | |||||||
chr15:40168070 | G | GA | 25 | a0001c0002t0001g0040 a0001c0002t0001g0041 a0001c0002t0001g0042 others(22): Show |
26 | HG01175.hp1 HG01516.hp1 HG01978.hp2 others(23): Show |
intron_variant | MODIFIER | c.180-1977dupA | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr15 | 40168070 | ||||||
chr15:40168070 | GA | G | 6 | a0001c0002t0001g0094 a0001c0003t0001g0158 a0001c0003t0001g0159 others(3): Show |
6 | NA18940.hp1 NA18983.hp2 NA19001.hp1 others(3): Show |
intron_variant | MODIFIER | c.180-1977delA | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr15 | 40168070 | ||||||
chr15:40168227 | C | T | 3 | a0002c0001t0002g0020 a0002c0001t0002g0221 a0002c0001t0002g0223 |
4 | NA18989.hp1 NA18993.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.180-1835C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40168227 | |||||||
chr15:40168347 | G | A | 4 | a0001c0003t0001g0158 a0001c0003t0001g0159 a0001c0003t0001g0161 others(1): Show |
4 | NA18940.hp1 NA18983.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.180-1715G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40168347 | |||||||
chr15:40168363 | G | A | 8 | a0001c0003t0001g0021 a0001c0003t0001g0168 a0001c0003t0001g0229 others(5): Show |
9 | HG02129.hp2 HG02165.hp2 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.180-1699G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40168363 | |||||||
chr15:40168426 | T | C | 3 | a0003c0005t0003g0123 a0003c0005t0003g0124 a0003c0005t0003g0128 |
3 | HG00642.hp2 HG02109.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.180-1636T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40168426 | |||||||
chr15:40168740 | T | A | 10 | a0001c0004t0001g0003 a0001c0004t0001g0129 a0001c0004t0001g0130 others(7): Show |
14 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.180-1322T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40168740 | |||||||
chr15:40168808 | C | T | 1 | a0001c0004t0001g0136 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.180-1254C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40168808 | |||||||
chr15:40169116 | T | C | 1 | a0001c0004t0001g0165 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.180-946T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40169116 | |||||||
chr15:40169609 | C | CT | 40 | a0001c0002t0001g0044 a0001c0002t0001g0093 a0001c0003t0001g0151 others(37): Show |
43 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.180-431dupT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr15 | 40169609 | ||||||
chr15:40169609 | C | CTT | 15 | a0001c0003t0001g0021 a0001c0003t0001g0158 a0001c0003t0001g0161 others(12): Show |
16 | HG01169.hp1 HG02129.hp2 HG02165.hp2 others(13): Show |
intron_variant | MODIFIER | c.180-432_180-431dup others(2): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr15 | 40169609 | ||||||
chr15:40169711 | C | A | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.180-351C>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40169711 | |||||||
chr15:40169720 | T | C | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.180-342T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40169720 | |||||||
chr15:40169794 | G | C | 6 | a0005c0007t0003g0005 a0005c0007t0003g0300 a0005c0007t0003g0301 others(3): Show |
9 | HG01081.hp1 HG01243.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.180-268G>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40169794 | |||||||
chr15:40169828 | G | T | 10 | a0001c0004t0001g0003 a0001c0004t0001g0129 a0001c0004t0001g0130 others(7): Show |
14 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.180-234G>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40169828 | |||||||
chr15:40170027 | A | G | 13 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0001g0149 others(10): Show |
13 | HG00741.hp2 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.180-35A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 2/22 | chr15 | 40170027 | |||||||
chr15:40170280 | G | A | 1 | a0002c0001t0002g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.239+159G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 3/22 | chr15 | 40170280 | |||||||
chr15:40170306 | T | G | 1 | a0001c0003t0001g0045 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.239+185T>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 3/22 | chr15 | 40170306 | |||||||
chr15:40170388 | A | G | 1 | a0011c0010t0001g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.240-149A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 3/22 | chr15 | 40170388 | |||||||
chr15:40170714 | A | C | 2 | a0001c0003t0001g0095 a0002c0001t0002g0295 |
2 | HG03239.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.384+33A>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40170714 | |||||||
chr15:40170736 | T | C | 1 | a0011c0010t0001g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.384+55T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40170736 | |||||||
chr15:40170805 | A | AT | 13 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0001g0149 others(10): Show |
13 | HG00741.hp2 HG02145.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.384+127dupT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr15 | 40170805 | ||||||
chr15:40170852 | G | T | 1 | a0001c0002t0001g0092 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.384+171G>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40170852 | |||||||
chr15:40170853 | A | T | 8 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0005c0007t0003g0005 others(5): Show |
11 | HG01081.hp1 HG01243.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.384+172A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40170853 | |||||||
chr15:40171013 | G | T | 1 | a0003c0005t0003g0146 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.384+332G>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40171013 | |||||||
chr15:40171047 | C | T | 1 | a0001c0002t0001g0091 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.384+366C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40171047 | |||||||
chr15:40171098 | A | T | 1 | a0002c0001t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.384+417A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40171098 | |||||||
chr15:40171365 | T | C | 1 | a0001c0002t0001g0046 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.384+684T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40171365 | |||||||
chr15:40171500 | T | A | 1 | a0002c0001t0002g0172 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.384+819T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40171500 | |||||||
chr15:40171556 | A | G | 109 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(106): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.384+875A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40171556 | |||||||
chr15:40171610 | A | G | 1 | a0001c0003t0001g0109 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.384+929A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40171610 | |||||||
chr15:40171620 | A | G | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.384+939A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40171620 | |||||||
chr15:40171736 | C | A | 2 | a0004c0006t0001g0032 a0004c0006t0001g0033 |
2 | HG02615.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.384+1055C>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40171736 | |||||||
chr15:40171931 | T | A | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.384+1250T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40171931 | |||||||
chr15:40172071 | TAAGAAAT others(18): Show |
T | 1 | a0011c0010t0001g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.384+1419_384+1443d others(27): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr15 | 40172071 | ||||||
chr15:40172120 | T | TAAAGTAA others(26): Show |
1 | a0002c0001t0002g0239 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.384+1476_384+1508d others(35): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr15 | 40172120 | ||||||
chr15:40172348 | T | A | 1 | a0001c0003t0001g0229 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.384+1667T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40172348 | |||||||
chr15:40172407 | C | T | 28 | a0001c0019t0003g0143 a0002c0001t0002g0265 a0003c0005t0003g0008 others(25): Show |
31 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.384+1726C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40172407 | |||||||
chr15:40172509 | T | C | 120 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(117): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(144): Show |
intron_variant | MODIFIER | c.384+1828T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40172509 | |||||||
chr15:40172661 | C | CTG | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.384+1982_384+1983d others(4): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr15 | 40172661 | ||||||
chr15:40172726 | AGAAAATT others(57): Show |
A | 1 | a0001c0002t0001g0107 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.384+2046_384+2109d others(66): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40172726 | |||||||
chr15:40172742 | C | G | 6 | a0005c0007t0003g0005 a0005c0007t0003g0300 a0005c0007t0003g0301 others(3): Show |
9 | HG01081.hp1 HG01243.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.384+2061C>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40172742 | |||||||
chr15:40172780 | C | T | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.384+2099C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40172780 | |||||||
chr15:40172971 | A | C | 13 | a0003c0005t0003g0008 a0003c0005t0003g0113 a0003c0005t0003g0118 others(10): Show |
15 | HG00642.hp2 HG02055.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.384+2290A>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40172971 | |||||||
chr15:40173048 | A | G | 179 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(176): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.384+2367A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40173048 | |||||||
chr15:40173092 | A | G | 10 | a0001c0004t0001g0003 a0001c0004t0001g0129 a0001c0004t0001g0130 others(7): Show |
14 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.384+2411A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40173092 | |||||||
chr15:40173145 | C | T | 2 | a0001c0002t0001g0035 a0001c0002t0001g0036 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.384+2464C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40173145 | |||||||
chr15:40173262 | C | T | 1 | a0004c0006t0002g0156 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.384+2581C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40173262 | |||||||
chr15:40173295 | T | TA | 73 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(70): Show |
89 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.384+2636dupA | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr15 | 40173295 | ||||||
chr15:40173295 | TA | T | 58 | a0001c0003t0001g0021 a0001c0003t0001g0027 a0001c0003t0001g0028 others(55): Show |
66 | HG00642.hp2 HG01109.hp1 HG01167.hp2 others(63): Show |
intron_variant | MODIFIER | c.384+2636delA | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | INFO_REALIGN_3_PRIME | chr15 | 40173295 | ||||||
chr15:40173704 | T | A | 195 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(192): Show |
231 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(228): Show |
intron_variant | MODIFIER | c.385-2773T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40173704 | |||||||
chr15:40173856 | T | A | 1 | a0001c0004t0001g0131 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.385-2621T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40173856 | |||||||
chr15:40174089 | A | G | 4 | a0001c0003t0001g0158 a0001c0003t0001g0159 a0001c0003t0001g0161 others(1): Show |
4 | NA18940.hp1 NA18983.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.385-2388A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40174089 | |||||||
chr15:40174468 | T | C | 1 | a0001c0003t0001g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.385-2009T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40174468 | |||||||
chr15:40174607 | A | G | 1 | a0009c0018t0003g0142 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.385-1870A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40174607 | |||||||
chr15:40174616 | A | G | 1 | a0001c0002t0001g0074 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.385-1861A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40174616 | |||||||
chr15:40174923 | C | A | 1 | a0002c0001t0002g0241 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.385-1554C>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40174923 | |||||||
chr15:40175447 | G | A | 1 | a0012c0017t0002g0174 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.385-1030G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40175447 | |||||||
chr15:40175893 | T | C | 18 | a0001c0004t0001g0024 a0001c0004t0001g0236 a0001c0004t0001g0281 others(15): Show |
19 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.385-584T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40175893 | |||||||
chr15:40176045 | C | T | 2 | a0001c0003t0001g0278 a0001c0003t0001g0279 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.385-432C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40176045 | |||||||
chr15:40176242 | C | T | 1 | a0002c0001t0002g0210 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.385-235C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40176242 | |||||||
chr15:40176243 | G | A | 1 | a0002c0001t0002g0242 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.385-234G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40176243 | |||||||
chr15:40176303 | C | T | 1 | a0002c0001t0002g0138 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.385-174C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40176303 | |||||||
chr15:40176354 | T | C | 8 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0005c0007t0003g0005 others(5): Show |
11 | HG01081.hp1 HG01243.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.385-123T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40176354 | |||||||
chr15:40176362 | T | C | 1 | a0008c0011t0001g0276 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.385-115T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40176362 | |||||||
chr15:40176413 | T | G | 4 | a0001c0002t0001g0006 a0001c0002t0001g0026 a0001c0002t0001g0029 others(1): Show |
6 | NA18954.hp2 NA18959.hp1 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.385-64T>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 4/22 | chr15 | 40176413 | |||||||
chr15:40176946 | A | G | 2 | a0004c0006t0002g0155 a0004c0006t0002g0157 |
2 | HG00741.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.581+273A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40176946 | |||||||
chr15:40177352 | T | C | 9 | a0004c0006t0001g0031 a0004c0006t0001g0032 a0004c0006t0001g0033 others(6): Show |
9 | HG00741.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.581+679T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40177352 | |||||||
chr15:40177513 | A | G | 35 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0001g0149 others(32): Show |
40 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.581+840A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40177513 | |||||||
chr15:40177555 | CTAT | C | 4 | a0001c0002t0001g0035 a0001c0002t0001g0036 a0001c0002t0001g0072 others(1): Show |
4 | HG03491.hp1 HG03492.hp1 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.581+887_581+889del others(3): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40177555 | ||||||
chr15:40177671 | C | A | 101 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(98): Show |
125 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.581+998C>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40177671 | |||||||
chr15:40178029 | AT | A | 59 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(56): Show |
75 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.581+1359delT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40178029 | ||||||
chr15:40178038 | AT | A | 36 | a0001c0002t0001g0047 a0001c0003t0001g0158 a0001c0003t0001g0159 others(33): Show |
39 | HG00642.hp2 HG00741.hp2 HG02055.hp1 others(36): Show |
intron_variant | MODIFIER | c.581+1379delT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40178038 | ||||||
chr15:40178219 | C | T | 1 | a0001c0003t0001g0234 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.581+1546C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40178219 | |||||||
chr15:40178953 | T | G | 1 | a0004c0006t0001g0033 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.581+2280T>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40178953 | |||||||
chr15:40179563 | T | C | 1 | a0002c0001t0002g0175 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.581+2890T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40179563 | |||||||
chr15:40179686 | C | T | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.581+3013C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40179686 | |||||||
chr15:40179892 | T | C | 4 | a0001c0003t0001g0158 a0001c0003t0001g0159 a0001c0003t0001g0161 others(1): Show |
4 | NA18940.hp1 NA18983.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.581+3219T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40179892 | |||||||
chr15:40179967 | C | CAT | 33 | a0001c0003t0001g0103 a0001c0003t0001g0147 a0001c0003t0001g0148 others(30): Show |
33 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.581+3315_581+3316d others(4): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40179967 | ||||||
chr15:40179967 | C | CATAT | 4 | a0001c0004t0001g0132 a0001c0004t0001g0284 a0001c0004t0001g0293 others(1): Show |
4 | HG01884.hp1 HG01975.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.581+3313_581+3316d others(6): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40179967 | ||||||
chr15:40179967 | C | CATATAT | 17 | a0001c0003t0001g0021 a0001c0003t0001g0168 a0001c0003t0001g0229 others(14): Show |
21 | HG01081.hp1 HG01168.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.581+3311_581+3316d others(8): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40179967 | ||||||
chr15:40179967 | C | CATATATA others(1): Show |
6 | a0001c0003t0001g0224 a0001c0003t0001g0226 a0001c0003t0001g0227 others(3): Show |
6 | HG01255.hp1 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.581+3309_581+3316d others(10): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40179967 | ||||||
chr15:40179967 | C | CATATATA others(3): Show |
2 | a0001c0003t0001g0152 a0001c0003t0001g0225 |
2 | HG02486.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.581+3307_581+3316d others(12): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40179967 | ||||||
chr15:40179967 | C | CATATATA others(5): Show |
1 | a0001c0003t0001g0151 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.581+3305_581+3316d others(14): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40179967 | ||||||
chr15:40179967 | CAT | C | 88 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(85): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.581+3315_581+3316d others(4): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40179967 | ||||||
chr15:40179986 | A | ATC | 4 | a0003c0005t0003g0016 a0003c0005t0003g0139 a0003c0005t0003g0141 others(1): Show |
5 | HG02280.hp1 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.581+3314_581+3315i others(4): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40179986 | ||||||
chr15:40179986 | A | C | 2 | a0002c0001t0002g0211 a0003c0005t0003g0140 |
2 | HG02717.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.581+3313A>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40179986 | |||||||
chr15:40179988 | A | ATC | 20 | a0001c0004t0001g0024 a0001c0004t0001g0282 a0003c0005t0003g0008 others(17): Show |
23 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.581+3319_581+3320d others(4): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40179988 | ||||||
chr15:40179988 | A | C | 11 | a0001c0002t0001g0163 a0001c0019t0003g0143 a0002c0001t0002g0211 others(8): Show |
12 | HG01175.hp1 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.581+3315A>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40179988 | |||||||
chr15:40180202 | C | T | 1 | a0001c0003t0001g0045 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.582-3512C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40180202 | |||||||
chr15:40180247 | GTTTCT | G | 8 | a0001c0003t0001g0027 a0001c0003t0001g0028 a0001c0003t0001g0085 others(5): Show |
8 | HG00099.hp1 HG01069.hp2 HG01123.hp1 others(5): Show |
intron_variant | MODIFIER | c.582-3463_582-3459d others(7): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40180247 | ||||||
chr15:40180251 | C | CT | 34 | a0001c0003t0001g0021 a0001c0003t0001g0168 a0001c0003t0001g0224 others(31): Show |
39 | HG01109.hp1 HG01123.hp2 HG01168.hp1 others(36): Show |
intron_variant | MODIFIER | c.582-3443dupT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40180251 | ||||||
chr15:40180251 | C | CTT | 22 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0001g0149 others(19): Show |
23 | HG00140.hp1 HG00735.hp2 HG01106.hp2 others(20): Show |
intron_variant | MODIFIER | c.582-3444_582-3443d others(4): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40180251 | ||||||
chr15:40180251 | C | CTTTTT | 22 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(19): Show |
24 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.582-3447_582-3443d others(7): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40180251 | ||||||
chr15:40180251 | C | CTTTTTT | 6 | a0003c0005t0003g0016 a0003c0005t0003g0126 a0003c0005t0003g0139 others(3): Show |
6 | HG02258.hp2 HG02280.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.582-3448_582-3443d others(8): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40180251 | ||||||
chr15:40180251 | CT | C | 108 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(105): Show |
135 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.582-3443delT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40180251 | ||||||
chr15:40180320 | C | T | 1 | a0002c0001t0002g0206 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.582-3394C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40180320 | |||||||
chr15:40180385 | G | A | 59 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(56): Show |
75 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(72): Show |
intron_variant | MODIFIER | c.582-3329G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40180385 | |||||||
chr15:40180451 | A | T | 4 | a0001c0019t0003g0143 a0003c0005t0003g0144 a0003c0005t0003g0145 others(1): Show |
4 | HG02145.hp2 HG02818.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.582-3263A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40180451 | |||||||
chr15:40180466 | A | G | 1 | a0001c0003t0001g0235 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.582-3248A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40180466 | |||||||
chr15:40180642 | C | T | 1 | a0002c0001t0002g0263 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.582-3072C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40180642 | |||||||
chr15:40180642 | CT | C | 120 | a0001c0002t0001g0067 a0001c0002t0001g0068 a0001c0002t0001g0073 others(117): Show |
133 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.582-3047delT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40180642 | ||||||
chr15:40180642 | CTT | C | 113 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(110): Show |
138 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.582-3048_582-3047d others(4): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40180642 | ||||||
chr15:40180642 | CTTT | C | 32 | a0001c0002t0001g0048 a0001c0002t0001g0075 a0001c0003t0001g0071 others(29): Show |
35 | HG00140.hp2 HG00642.hp2 HG01168.hp1 others(32): Show |
intron_variant | MODIFIER | c.582-3049_582-3047d others(5): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40180642 | ||||||
chr15:40180642 | CTTTTTTT others(1): Show |
C | 6 | a0005c0007t0003g0005 a0005c0007t0003g0300 a0005c0007t0003g0301 others(3): Show |
9 | HG01081.hp1 HG01243.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.582-3054_582-3047d others(10): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40180642 | ||||||
chr15:40180642 | CTTTTTTT others(5): Show |
C | 1 | a0001c0003t0001g0231 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.582-3058_582-3047d others(14): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40180642 | ||||||
chr15:40180642 | CTTTTTTT others(6): Show |
C | 1 | a0001c0004t0001g0165 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.582-3059_582-3047d others(15): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40180642 | ||||||
chr15:40180642 | CTTTTTTT others(8): Show |
C | 4 | a0001c0003t0001g0158 a0001c0003t0001g0159 a0001c0003t0001g0161 others(1): Show |
4 | NA18940.hp1 NA18983.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.582-3061_582-3047d others(17): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40180642 | ||||||
chr15:40180650 | T | C | 2 | a0001c0003t0001g0151 a0001c0003t0001g0152 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.582-3064T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40180650 | |||||||
chr15:40180699 | C | G | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.582-3015C>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40180699 | |||||||
chr15:40180840 | G | A | 1 | a0011c0010t0001g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.582-2874G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40180840 | |||||||
chr15:40181093 | AT | A | 162 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(159): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.582-2604delT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40181093 | ||||||
chr15:40181133 | C | G | 10 | a0001c0004t0001g0003 a0001c0004t0001g0129 a0001c0004t0001g0130 others(7): Show |
14 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.582-2581C>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40181133 | |||||||
chr15:40181294 | T | C | 105 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(102): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.582-2420T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40181294 | |||||||
chr15:40181368 | G | C | 1 | a0002c0001t0002g0171 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.582-2346G>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40181368 | |||||||
chr15:40181399 | G | A | 191 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(188): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.582-2315G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40181399 | |||||||
chr15:40181500 | AT | A | 105 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(102): Show |
129 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(126): Show |
intron_variant | MODIFIER | c.582-2208delT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr15 | 40181500 | ||||||
chr15:40181539 | G | C | 1 | a0003c0005t0003g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.582-2175G>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40181539 | |||||||
chr15:40181693 | T | C | 11 | a0001c0003t0001g0021 a0001c0003t0001g0168 a0001c0003t0001g0229 others(8): Show |
12 | HG01168.hp1 HG01169.hp1 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.582-2021T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40181693 | |||||||
chr15:40181975 | G | A | 4 | a0001c0003t0001g0158 a0001c0003t0001g0159 a0001c0003t0001g0161 others(1): Show |
4 | NA18940.hp1 NA18983.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.582-1739G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40181975 | |||||||
chr15:40182195 | C | G | 18 | a0001c0004t0001g0024 a0001c0004t0001g0236 a0001c0004t0001g0281 others(15): Show |
19 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.582-1519C>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40182195 | |||||||
chr15:40182536 | C | G | 1 | a0001c0003t0001g0038 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.582-1178C>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40182536 | |||||||
chr15:40182708 | C | A | 2 | a0001c0003t0001g0151 a0001c0003t0001g0152 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.582-1006C>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40182708 | |||||||
chr15:40182827 | T | A | 1 | a0001c0002t0001g0074 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.582-887T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40182827 | |||||||
chr15:40182833 | A | G | 2 | a0004c0006t0001g0031 a0004c0006t0001g0034 |
2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.582-881A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40182833 | |||||||
chr15:40182972 | G | T | 140 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(137): Show |
170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.582-742G>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40182972 | |||||||
chr15:40183020 | G | A | 5 | a0001c0002t0001g0044 a0001c0002t0001g0049 a0001c0002t0001g0066 others(2): Show |
5 | NA18962.hp1 NA18984.hp2 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.582-694G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40183020 | |||||||
chr15:40183029 | C | T | 2 | a0001c0003t0001g0014 a0001c0003t0001g0084 |
3 | HG00621.hp2 NA18945.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.582-685C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40183029 | |||||||
chr15:40183077 | T | C | 22 | a0002c0001t0002g0023 a0002c0001t0002g0111 a0002c0001t0002g0167 others(19): Show |
23 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(20): Show |
intron_variant | MODIFIER | c.582-637T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40183077 | |||||||
chr15:40183281 | G | A | 1 | a0002c0001t0002g0247 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.582-433G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40183281 | |||||||
chr15:40183287 | G | A | 1 | a0001c0004t0001g0285 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.582-427G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40183287 | |||||||
chr15:40183291 | G | A | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.582-423G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40183291 | |||||||
chr15:40183490 | C | G | 1 | a0002c0001t0002g0209 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.582-224C>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 5/22 | chr15 | 40183490 | |||||||
chr15:40183898 | C | T | 4 | a0001c0003t0001g0158 a0001c0003t0001g0159 a0001c0003t0001g0161 others(1): Show |
4 | NA18940.hp1 NA18983.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.751+15C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 6/22 | chr15 | 40183898 | |||||||
chr15:40183930 | T | TA | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.751+51dupA | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr15 | 40183930 | ||||||
chr15:40184147 | T | C | 2 | a0002c0001t0002g0199 a0002c0001t0002g0200 |
2 | NA18977.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.751+264T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 6/22 | chr15 | 40184147 | |||||||
chr15:40184185 | A | G | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.751+302A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 6/22 | chr15 | 40184185 | |||||||
chr15:40184227 | C | T | 1 | a0001c0004t0001g0284 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.751+344C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 6/22 | chr15 | 40184227 | |||||||
chr15:40184309 | G | A | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.751+426G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 6/22 | chr15 | 40184309 | |||||||
chr15:40184311 | A | G | 2 | a0004c0006t0002g0154 a0004c0006t0002g0156 |
2 | HG02647.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.751+428A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 6/22 | chr15 | 40184311 | |||||||
chr15:40184312 | C | CTT | 29 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0001c0019t0003g0143 others(26): Show |
32 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(29): Show |
intron_variant | MODIFIER | c.751+441_751+442dup others(2): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 6/22 | INFO_REALIGN_3_PRIME | chr15 | 40184312 | ||||||
chr15:40184364 | G | A | 1 | a0001c0003t0001g0226 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.751+481G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 6/22 | chr15 | 40184364 | |||||||
chr15:40184641 | T | A | 35 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0001g0149 others(32): Show |
40 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.752-524T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 6/22 | chr15 | 40184641 | |||||||
chr15:40184670 | G | A | 31 | a0001c0004t0001g0003 a0001c0004t0001g0024 a0001c0004t0001g0129 others(28): Show |
36 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.752-495G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 6/22 | chr15 | 40184670 | |||||||
chr15:40184674 | T | A | 1 | a0001c0002t0001g0050 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.752-491T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 6/22 | chr15 | 40184674 | |||||||
chr15:40184964 | A | T | 1 | a0011c0010t0001g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.752-201A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 6/22 | chr15 | 40184964 | |||||||
chr15:40184979 | G | C | 1 | a0002c0016t0002g0252 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.752-186G>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 6/22 | chr15 | 40184979 | |||||||
chr15:40185121 | A | G | 2 | a0002c0001t0002g0197 a0002c0001t0002g0217 |
2 | HG00741.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.752-44A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 6/22 | chr15 | 40185121 | |||||||
chr15:40185734 | G | C | 2 | a0001c0003t0001g0151 a0001c0003t0001g0152 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1058+92G>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40185734 | |||||||
chr15:40185791 | C | G | 1 | a0008c0011t0001g0276 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1058+149C>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40185791 | |||||||
chr15:40185869 | A | T | 1 | a0002c0001t0001g0164 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1058+227A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40185869 | |||||||
chr15:40186236 | G | A | 1 | a0001c0002t0001g0026 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1058+594G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40186236 | |||||||
chr15:40186376 | G | A | 18 | a0001c0004t0001g0024 a0001c0004t0001g0236 a0001c0004t0001g0281 others(15): Show |
19 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1058+734G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40186376 | |||||||
chr15:40186430 | C | CT | 134 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(131): Show |
163 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.1058+813dupT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr15 | 40186430 | ||||||
chr15:40186430 | C | CTT | 19 | a0001c0002t0001g0064 a0001c0002t0001g0065 a0001c0002t0001g0093 others(16): Show |
22 | HG01081.hp1 HG01169.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.1058+812_1058+813d others(4): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr15 | 40186430 | ||||||
chr15:40186430 | C | CTTT | 18 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0113 others(15): Show |
20 | HG00642.hp2 HG01243.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1058+811_1058+813d others(5): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr15 | 40186430 | ||||||
chr15:40186430 | C | CTTTT | 7 | a0003c0005t0003g0016 a0003c0005t0003g0116 a0003c0005t0003g0122 others(4): Show |
8 | HG02055.hp1 HG02055.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1058+810_1058+813d others(6): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr15 | 40186430 | ||||||
chr15:40186430 | CT | C | 9 | a0001c0004t0001g0284 a0002c0001t0001g0101 a0002c0001t0001g0253 others(6): Show |
9 | HG01257.hp2 HG01496.hp2 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.1058+813delT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr15 | 40186430 | ||||||
chr15:40186472 | G | C | 176 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(173): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1058+830G>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40186472 | |||||||
chr15:40186508 | G | A | 1 | a0002c0001t0005g0275 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1058+866G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40186508 | |||||||
chr15:40186511 | C | T | 1 | a0001c0002t0001g0043 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1058+869C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40186511 | |||||||
chr15:40186577 | T | C | 60 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0001g0149 others(57): Show |
71 | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.1058+935T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40186577 | |||||||
chr15:40186652 | A | G | 5 | a0001c0003t0001g0158 a0001c0003t0001g0159 a0001c0003t0001g0161 others(2): Show |
5 | HG01884.hp1 NA18940.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.1058+1010A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40186652 | |||||||
chr15:40186692 | G | A | 257 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(254): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1058+1050G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40186692 | |||||||
chr15:40186715 | A | G | 1 | a0001c0002t0001g0091 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1058+1073A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40186715 | |||||||
chr15:40186734 | T | C | 183 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(180): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.1058+1092T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40186734 | |||||||
chr15:40186735 | G | A | 2 | a0002c0001t0002g0181 a0011c0010t0001g0277 |
2 | HG00609.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1058+1093G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40186735 | |||||||
chr15:40186736 | C | T | 24 | a0001c0003t0001g0224 a0001c0004t0001g0236 a0001c0004t0001g0281 others(21): Show |
24 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.1058+1094C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40186736 | |||||||
chr15:40186903 | C | CT | 16 | a0001c0003t0001g0021 a0001c0003t0001g0168 a0001c0003t0001g0224 others(13): Show |
17 | HG01168.hp1 HG01169.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.1058+1274dupT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr15 | 40186903 | ||||||
chr15:40186916 | T | C | 1 | a0002c0001t0002g0245 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1058+1274T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40186916 | |||||||
chr15:40187130 | A | AT | 192 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(189): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1058+1501dupT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr15 | 40187130 | ||||||
chr15:40187152 | G | C | 4 | a0001c0003t0001g0158 a0001c0003t0001g0159 a0001c0003t0001g0161 others(1): Show |
4 | NA18940.hp1 NA18983.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1058+1510G>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40187152 | |||||||
chr15:40187156 | T | C | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1058+1514T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40187156 | |||||||
chr15:40187169 | A | G | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1058+1527A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40187169 | |||||||
chr15:40187187 | A | G | 1 | a0004c0006t0002g0153 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1058+1545A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40187187 | |||||||
chr15:40187227 | G | T | 1 | a0002c0001t0002g0195 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1058+1585G>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40187227 | |||||||
chr15:40187306 | T | G | 2 | a0001c0003t0001g0151 a0001c0003t0001g0152 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1058+1664T>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40187306 | |||||||
chr15:40187315 | A | T | 6 | a0005c0007t0003g0005 a0005c0007t0003g0300 a0005c0007t0003g0301 others(3): Show |
9 | HG01081.hp1 HG01243.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1058+1673A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40187315 | |||||||
chr15:40187328 | G | A | 2 | a0001c0003t0001g0151 a0001c0003t0001g0152 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1058+1686G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40187328 | |||||||
chr15:40187348 | G | A | 18 | a0001c0004t0001g0024 a0001c0004t0001g0236 a0001c0004t0001g0281 others(15): Show |
19 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.1058+1706G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40187348 | |||||||
chr15:40187415 | C | T | 2 | a0001c0003t0001g0151 a0001c0003t0001g0152 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1058+1773C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40187415 | |||||||
chr15:40187449 | G | C | 1 | a0011c0010t0001g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1058+1807G>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40187449 | |||||||
chr15:40187613 | A | G | 1 | a0002c0001t0002g0272 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1058+1971A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40187613 | |||||||
chr15:40187638 | G | A | 192 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(189): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1058+1996G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40187638 | |||||||
chr15:40187953 | G | T | 192 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(189): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1058+2311G>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40187953 | |||||||
chr15:40188171 | C | T | 1 | a0002c0001t0002g0215 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.1058+2529C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40188171 | |||||||
chr15:40188280 | T | C | 1 | a0001c0003t0001g0085 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1058+2638T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40188280 | |||||||
chr15:40188377 | A | G | 2 | a0001c0003t0001g0151 a0001c0003t0001g0152 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1058+2735A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40188377 | |||||||
chr15:40188414 | T | A | 4 | a0001c0003t0001g0012 a0001c0003t0001g0013 a0001c0003t0001g0069 others(1): Show |
6 | HG02523.hp2 NA18747.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.1058+2772T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40188414 | |||||||
chr15:40188582 | C | CT | 54 | a0001c0002t0001g0068 a0001c0003t0001g0147 a0001c0003t0001g0148 others(51): Show |
58 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.1058+2957dupT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr15 | 40188582 | ||||||
chr15:40188582 | CT | C | 6 | a0001c0002t0001g0107 a0001c0003t0006g0160 a0001c0004t0001g0133 others(3): Show |
6 | HG02896.hp1 HG03098.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1058+2957delT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr15 | 40188582 | ||||||
chr15:40188600 | C | T | 1 | a0002c0001t0002g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1058+2958C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40188600 | |||||||
chr15:40188672 | T | G | 1 | a0001c0004t0001g0290 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1058+3030T>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40188672 | |||||||
chr15:40188697 | C | T | 16 | a0001c0003t0001g0021 a0001c0003t0001g0168 a0001c0003t0001g0224 others(13): Show |
17 | HG01168.hp1 HG01169.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.1058+3055C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40188697 | |||||||
chr15:40188727 | C | T | 1 | a0011c0010t0001g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1058+3085C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40188727 | |||||||
chr15:40188867 | C | T | 1 | a0002c0001t0002g0194 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1058+3225C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40188867 | |||||||
chr15:40188957 | T | C | 4 | a0001c0003t0001g0158 a0001c0003t0001g0159 a0001c0003t0001g0161 others(1): Show |
4 | NA18940.hp1 NA18983.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1058+3315T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40188957 | |||||||
chr15:40189036 | C | T | 1 | a0002c0001t0002g0178 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1058+3394C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40189036 | |||||||
chr15:40189160 | T | A | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1058+3518T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40189160 | |||||||
chr15:40189372 | C | G | 1 | a0002c0001t0002g0177 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1058+3730C>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40189372 | |||||||
chr15:40189377 | C | T | 1 | a0001c0004t0001g0133 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1058+3735C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40189377 | |||||||
chr15:40189406 | C | T | 2 | a0001c0003t0001g0151 a0001c0003t0001g0152 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1058+3764C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40189406 | |||||||
chr15:40189424 | C | T | 156 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(153): Show |
187 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1058+3782C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40189424 | |||||||
chr15:40189451 | C | T | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1058+3809C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40189451 | |||||||
chr15:40189456 | A | G | 192 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(189): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1058+3814A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40189456 | |||||||
chr15:40189496 | G | A | 43 | a0001c0003t0001g0021 a0001c0003t0001g0168 a0001c0003t0001g0224 others(40): Show |
47 | HG00642.hp2 HG01168.hp1 HG01169.hp1 others(44): Show |
intron_variant | MODIFIER | c.1058+3854G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40189496 | |||||||
chr15:40189541 | C | T | 8 | a0002c0001t0002g0173 a0002c0001t0002g0177 a0002c0001t0002g0178 others(5): Show |
8 | HG01496.hp2 HG01891.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.1058+3899C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40189541 | |||||||
chr15:40189589 | A | G | 16 | a0001c0003t0001g0021 a0001c0003t0001g0168 a0001c0003t0001g0224 others(13): Show |
17 | HG01168.hp1 HG01169.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.1058+3947A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40189589 | |||||||
chr15:40189707 | G | A | 1 | a0001c0004t0001g0133 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1058+4065G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40189707 | |||||||
chr15:40189716 | G | A | 2 | a0001c0003t0001g0224 a0001c0003t0001g0226 |
2 | HG01255.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1058+4074G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40189716 | |||||||
chr15:40189721 | T | C | 3 | a0002c0001t0002g0242 a0002c0001t0002g0244 a0002c0001t0002g0245 |
3 | NA18747.hp2 NA18950.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.1058+4079T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40189721 | |||||||
chr15:40189726 | C | G | 1 | a0002c0001t0002g0190 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1058+4084C>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40189726 | |||||||
chr15:40189949 | G | A | 191 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(188): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.1058+4307G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40189949 | |||||||
chr15:40190208 | T | C | 2 | a0002c0001t0002g0260 a0002c0001t0002g0272 |
2 | HG02148.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1058+4566T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40190208 | |||||||
chr15:40190293 | T | G | 6 | a0005c0007t0003g0005 a0005c0007t0003g0300 a0005c0007t0003g0301 others(3): Show |
9 | HG01081.hp1 HG01243.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1058+4651T>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40190293 | |||||||
chr15:40190359 | A | G | 6 | a0005c0007t0003g0005 a0005c0007t0003g0300 a0005c0007t0003g0301 others(3): Show |
9 | HG01081.hp1 HG01243.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1058+4717A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40190359 | |||||||
chr15:40190484 | C | T | 1 | a0002c0001t0002g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1058+4842C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40190484 | |||||||
chr15:40190548 | C | T | 17 | a0003c0005t0003g0008 a0003c0005t0003g0113 a0003c0005t0003g0114 others(14): Show |
19 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.1058+4906C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40190548 | |||||||
chr15:40190549 | G | A | 1 | a0008c0011t0001g0276 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1058+4907G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40190549 | |||||||
chr15:40190585 | C | G | 43 | a0001c0003t0001g0021 a0001c0003t0001g0168 a0001c0003t0001g0224 others(40): Show |
47 | HG00642.hp2 HG01168.hp1 HG01169.hp1 others(44): Show |
intron_variant | MODIFIER | c.1058+4943C>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40190585 | |||||||
chr15:40190888 | A | AT | 52 | a0001c0002t0001g0094 a0001c0003t0001g0021 a0001c0003t0001g0168 others(49): Show |
59 | HG00642.hp2 HG01081.hp1 HG01168.hp1 others(56): Show |
intron_variant | MODIFIER | c.1058+5263dupT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr15 | 40190888 | ||||||
chr15:40190912 | G | A | 4 | a0002c0001t0002g0017 a0002c0001t0002g0195 a0002c0001t0002g0197 others(1): Show |
5 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.1058+5270G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40190912 | |||||||
chr15:40190938 | A | C | 4 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0001g0149 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1058+5296A>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40190938 | |||||||
chr15:40190981 | G | A | 11 | a0001c0003t0001g0021 a0001c0003t0001g0168 a0001c0003t0001g0229 others(8): Show |
12 | HG01168.hp1 HG01169.hp1 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.1058+5339G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40190981 | |||||||
chr15:40191024 | A | G | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1058+5382A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40191024 | |||||||
chr15:40191162 | A | G | 16 | a0001c0003t0001g0021 a0001c0003t0001g0168 a0001c0003t0001g0224 others(13): Show |
17 | HG01168.hp1 HG01169.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.1059-5383A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40191162 | |||||||
chr15:40191324 | T | C | 1 | a0001c0002t0001g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1059-5221T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40191324 | |||||||
chr15:40191745 | T | C | 16 | a0001c0003t0001g0021 a0001c0003t0001g0168 a0001c0003t0001g0224 others(13): Show |
17 | HG01168.hp1 HG01169.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.1059-4800T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40191745 | |||||||
chr15:40191821 | T | C | 1 | a0008c0011t0001g0276 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1059-4724T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40191821 | |||||||
chr15:40191880 | G | T | 10 | a0001c0004t0001g0003 a0001c0004t0001g0129 a0001c0004t0001g0130 others(7): Show |
14 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1059-4665G>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40191880 | |||||||
chr15:40191925 | G | A | 1 | a0001c0003t0001g0226 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1059-4620G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40191925 | |||||||
chr15:40191930 | A | C | 4 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0001g0149 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059-4615A>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40191930 | |||||||
chr15:40191933 | C | G | 33 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(30): Show |
39 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.1059-4612C>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40191933 | |||||||
chr15:40192351 | G | A | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1059-4194G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40192351 | |||||||
chr15:40192416 | T | C | 1 | a0001c0003t0001g0234 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1059-4129T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40192416 | |||||||
chr15:40192515 | A | G | 1 | a0004c0006t0002g0156 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1059-4030A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40192515 | |||||||
chr15:40192601 | C | G | 16 | a0001c0003t0001g0021 a0001c0003t0001g0168 a0001c0003t0001g0224 others(13): Show |
17 | HG01168.hp1 HG01169.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.1059-3944C>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40192601 | |||||||
chr15:40192704 | C | T | 1 | a0002c0001t0002g0296 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1059-3841C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40192704 | |||||||
chr15:40192827 | A | G | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1059-3718A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40192827 | |||||||
chr15:40192892 | C | T | 1 | a0002c0001t0002g0198 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1059-3653C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40192892 | |||||||
chr15:40192977 | A | G | 1 | a0004c0006t0001g0032 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1059-3568A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40192977 | |||||||
chr15:40193004 | C | T | 1 | a0002c0001t0002g0208 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1059-3541C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40193004 | |||||||
chr15:40193008 | GGCTGGCT others(39): Show |
G | 1 | a0011c0010t0001g0277 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1059-3534_1059-348 others(50): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr15 | 40193008 | ||||||
chr15:40193023 | T | A | 1 | a0001c0002t0001g0001 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1059-3522T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40193023 | |||||||
chr15:40193253 | A | G | 107 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(104): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(128): Show |
intron_variant | MODIFIER | c.1059-3292A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40193253 | |||||||
chr15:40193280 | C | G | 1 | a0002c0001t0002g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1059-3265C>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40193280 | |||||||
chr15:40193435 | T | C | 295 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(292): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.1059-3110T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40193435 | |||||||
chr15:40193439 | CT | C | 106 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(103): Show |
130 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(127): Show |
intron_variant | MODIFIER | c.1059-3093delT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr15 | 40193439 | ||||||
chr15:40193451 | T | A | 2 | a0001c0004t0001g0137 a0002c0001t0002g0272 |
2 | HG02735.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1059-3094T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40193451 | |||||||
chr15:40193468 | C | CT | 56 | a0001c0002t0001g0011 a0001c0002t0001g0042 a0001c0002t0001g0051 others(53): Show |
60 | HG00099.hp1 HG00642.hp2 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.1059-3053dupT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr15 | 40193468 | ||||||
chr15:40193468 | C | CTT | 9 | a0001c0003t0001g0071 a0001c0003t0001g0158 a0001c0019t0003g0143 others(6): Show |
9 | HG00140.hp2 HG02055.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059-3054_1059-305 others(6): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr15 | 40193468 | ||||||
chr15:40193468 | CT | C | 9 | a0001c0002t0001g0107 a0001c0003t0001g0038 a0001c0003t0001g0147 others(6): Show |
9 | HG01255.hp2 HG01516.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059-3053delT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr15 | 40193468 | ||||||
chr15:40193468 | CTTTTTTT others(4): Show |
C | 9 | a0004c0006t0001g0031 a0004c0006t0001g0032 a0004c0006t0001g0033 others(6): Show |
9 | HG00741.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1059-3063_1059-305 others(15): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr15 | 40193468 | ||||||
chr15:40193602 | AT | A | 4 | a0001c0002t0001g0007 a0001c0002t0001g0053 a0001c0002t0001g0093 others(1): Show |
6 | HG00280.hp1 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1059-2933delT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr15 | 40193602 | ||||||
chr15:40193703 | C | T | 10 | a0001c0004t0001g0003 a0001c0004t0001g0129 a0001c0004t0001g0130 others(7): Show |
14 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1059-2842C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40193703 | |||||||
chr15:40193729 | A | G | 1 | a0002c0001t0002g0295 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1059-2816A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40193729 | |||||||
chr15:40193840 | A | G | 192 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(189): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1059-2705A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40193840 | |||||||
chr15:40193893 | T | TAA | 25 | a0001c0004t0001g0165 a0001c0019t0003g0143 a0003c0005t0003g0008 others(22): Show |
28 | HG00642.hp2 HG01109.hp1 HG02109.hp2 others(25): Show |
intron_variant | MODIFIER | c.1059-2636_1059-263 others(6): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr15 | 40193893 | ||||||
chr15:40193893 | TA | T | 7 | a0001c0003t0006g0160 a0005c0007t0003g0005 a0005c0007t0003g0300 others(4): Show |
10 | HG01081.hp1 HG01243.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1059-2635delA | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr15 | 40193893 | ||||||
chr15:40193928 | G | T | 2 | a0001c0002t0001g0035 a0001c0002t0001g0036 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1059-2617G>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40193928 | |||||||
chr15:40194052 | A | C | 2 | a0003c0005t0003g0121 a0003c0005t0003g0122 |
2 | HG02055.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1059-2493A>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40194052 | |||||||
chr15:40194054 | T | A | 35 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0001g0149 others(32): Show |
40 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1059-2491T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40194054 | |||||||
chr15:40194109 | TA | T | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1059-2434delA | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr15 | 40194109 | ||||||
chr15:40194115 | C | T | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1059-2430C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40194115 | |||||||
chr15:40194117 | T | A | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1059-2428T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40194117 | |||||||
chr15:40194285 | A | G | 1 | a0001c0003t0001g0109 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1059-2260A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40194285 | |||||||
chr15:40194465 | G | A | 35 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0001g0149 others(32): Show |
40 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1059-2080G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40194465 | |||||||
chr15:40194491 | G | T | 16 | a0001c0003t0001g0021 a0001c0003t0001g0168 a0001c0003t0001g0224 others(13): Show |
17 | HG01168.hp1 HG01169.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.1059-2054G>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40194491 | |||||||
chr15:40194801 | C | G | 6 | a0005c0007t0003g0005 a0005c0007t0003g0300 a0005c0007t0003g0301 others(3): Show |
9 | HG01081.hp1 HG01243.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1059-1744C>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40194801 | |||||||
chr15:40194805 | A | C | 1 | a0001c0002t0001g0060 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1059-1740A>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40194805 | |||||||
chr15:40195018 | C | T | 33 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(30): Show |
39 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.1059-1527C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40195018 | |||||||
chr15:40195054 | G | A | 4 | a0001c0003t0001g0158 a0001c0003t0001g0159 a0001c0003t0001g0161 others(1): Show |
4 | NA18940.hp1 NA18983.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059-1491G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40195054 | |||||||
chr15:40195120 | T | C | 33 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(30): Show |
39 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.1059-1425T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40195120 | |||||||
chr15:40195466 | A | G | 2 | a0001c0003t0001g0151 a0001c0003t0001g0152 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1059-1079A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40195466 | |||||||
chr15:40195482 | C | T | 1 | a0001c0002t0001g0042 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1059-1063C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40195482 | |||||||
chr15:40195573 | G | T | 1 | a0001c0002t0001g0059 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1059-972G>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40195573 | |||||||
chr15:40195603 | T | C | 1 | a0002c0001t0002g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1059-942T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40195603 | |||||||
chr15:40195772 | G | A | 2 | a0001c0004t0001g0283 a0001c0004t0001g0287 |
2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1059-773G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40195772 | |||||||
chr15:40195926 | G | A | 1 | a0001c0003t0001g0225 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1059-619G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40195926 | |||||||
chr15:40196253 | A | T | 2 | a0001c0004t0004g0298 a0001c0004t0004g0299 |
2 | HG00735.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1059-292A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40196253 | |||||||
chr15:40196260 | G | A | 108 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(105): Show |
132 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(129): Show |
intron_variant | MODIFIER | c.1059-285G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40196260 | |||||||
chr15:40196367 | A | G | 33 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(30): Show |
39 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.1059-178A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40196367 | |||||||
chr15:40196535 | G | A | 2 | a0002c0001t0002g0199 a0002c0001t0002g0200 |
2 | NA18977.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.1059-10G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 8/22 | chr15 | 40196535 | |||||||
chr15:40196890 | A | G | 1 | a0003c0020t0003g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1288+116A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 9/22 | chr15 | 40196890 | |||||||
chr15:40196985 | G | T | 10 | a0001c0004t0001g0003 a0001c0004t0001g0129 a0001c0004t0001g0130 others(7): Show |
14 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1288+211G>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 9/22 | chr15 | 40196985 | |||||||
chr15:40197008 | G | A | 1 | a0001c0002t0001g0099 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1288+234G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 9/22 | chr15 | 40197008 | |||||||
chr15:40197099 | A | G | 1 | a0002c0001t0001g0101 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1288+325A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 9/22 | chr15 | 40197099 | |||||||
chr15:40197186 | C | T | 33 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(30): Show |
39 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.1288+412C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 9/22 | chr15 | 40197186 | |||||||
chr15:40197357 | A | G | 2 | a0001c0003t0001g0151 a0001c0003t0001g0152 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1288+583A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 9/22 | chr15 | 40197357 | |||||||
chr15:40197481 | T | C | 1 | a0002c0001t0002g0193 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1288+707T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 9/22 | chr15 | 40197481 | |||||||
chr15:40197865 | G | T | 1 | a0001c0002t0001g0060 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1288+1091G>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 9/22 | chr15 | 40197865 | |||||||
chr15:40198106 | C | T | 2 | a0002c0001t0002g0257 a0002c0001t0002g0258 |
2 | HG02155.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.1288+1332C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 9/22 | chr15 | 40198106 | |||||||
chr15:40198239 | G | GT | 148 | a0001c0003t0001g0095 a0001c0003t0001g0147 a0001c0003t0001g0148 others(145): Show |
163 | HG00140.hp1 HG00280.hp2 HG00408.hp2 others(160): Show |
intron_variant | MODIFIER | c.1289-1362dupT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr15 | 40198239 | ||||||
chr15:40198239 | G | GTT | 33 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(30): Show |
39 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.1289-1363_1289-136 others(6): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 9/22 | INFO_REALIGN_3_PRIME | chr15 | 40198239 | ||||||
chr15:40198510 | A | G | 175 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(172): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.1289-1105A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 9/22 | chr15 | 40198510 | |||||||
chr15:40199053 | C | T | 9 | a0004c0006t0001g0031 a0004c0006t0001g0032 a0004c0006t0001g0033 others(6): Show |
9 | HG00741.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1289-562C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 9/22 | chr15 | 40199053 | |||||||
chr15:40199242 | A | G | 1 | a0001c0003t0001g0089 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1289-373A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 9/22 | chr15 | 40199242 | |||||||
chr15:40199469 | G | A | 10 | a0001c0004t0001g0003 a0001c0004t0001g0129 a0001c0004t0001g0130 others(7): Show |
14 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1289-146G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 9/22 | chr15 | 40199469 | |||||||
chr15:40199572 | T | C | 5 | a0001c0003t0001g0224 a0001c0003t0001g0225 a0001c0003t0001g0226 others(2): Show |
5 | HG01255.hp1 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1289-43T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 9/22 | chr15 | 40199572 | |||||||
chr15:40199751 | A | G | 95 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(92): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.1401+24A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 10/22 | chr15 | 40199751 | |||||||
chr15:40199816 | C | T | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1401+89C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 10/22 | chr15 | 40199816 | |||||||
chr15:40199870 | C | T | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1401+143C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 10/22 | chr15 | 40199870 | |||||||
chr15:40200042 | T | C | 4 | a0001c0003t0001g0158 a0001c0003t0001g0159 a0001c0003t0001g0161 others(1): Show |
4 | NA18940.hp1 NA18983.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1402-202T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 10/22 | chr15 | 40200042 | |||||||
chr15:40200120 | G | T | 2 | a0001c0002t0001g0058 a0001c0002t0001g0078 |
2 | HG01069.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1402-124G>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 10/22 | chr15 | 40200120 | |||||||
chr15:40200131 | T | C | 1 | a0001c0004t0001g0165 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1402-113T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 10/22 | chr15 | 40200131 | |||||||
chr15:40200204 | G | A | 11 | a0001c0004t0001g0003 a0001c0004t0001g0129 a0001c0004t0001g0130 others(8): Show |
15 | HG01109.hp1 HG02257.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1402-40G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 10/22 | chr15 | 40200204 | |||||||
chr15:40200476 | T | A | 11 | a0001c0004t0001g0003 a0001c0004t0001g0129 a0001c0004t0001g0130 others(8): Show |
15 | HG01109.hp1 HG02257.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1517+117T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 11/22 | chr15 | 40200476 | |||||||
chr15:40200619 | A | T | 1 | a0002c0001t0002g0262 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1517+260A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 11/22 | chr15 | 40200619 | |||||||
chr15:40201063 | A | G | 1 | a0001c0004t0001g0132 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1567+83A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 12/22 | chr15 | 40201063 | |||||||
chr15:40201140 | T | C | 1 | a0003c0005t0003g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1567+160T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 12/22 | chr15 | 40201140 | |||||||
chr15:40201291 | A | G | 35 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0001g0149 others(32): Show |
40 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1567+311A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 12/22 | chr15 | 40201291 | |||||||
chr15:40201306 | A | G | 1 | a0002c0001t0002g0208 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1567+326A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 12/22 | chr15 | 40201306 | |||||||
chr15:40201658 | T | A | 1 | a0001c0003t0001g0069 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1567+678T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 12/22 | chr15 | 40201658 | |||||||
chr15:40201744 | A | G | 1 | a0001c0004t0001g0133 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1568-661A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 12/22 | chr15 | 40201744 | |||||||
chr15:40201811 | C | T | 27 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(24): Show |
30 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.1568-594C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 12/22 | chr15 | 40201811 | |||||||
chr15:40201911 | C | T | 1 | a0002c0001t0002g0222 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1568-494C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 12/22 | chr15 | 40201911 | |||||||
chr15:40202297 | G | A | 142 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(139): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1568-108G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 12/22 | chr15 | 40202297 | |||||||
chr15:40202372 | C | T | 1 | a0001c0002t0001g0062 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1568-33C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 12/22 | chr15 | 40202372 | |||||||
chr15:40202480 | T | G | 1 | a0002c0001t0002g0243 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1628+15T>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 13/22 | chr15 | 40202480 | |||||||
chr15:40202490 | G | T | 1 | a0001c0002t0001g0057 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1628+25G>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 13/22 | chr15 | 40202490 | |||||||
chr15:40202530 | G | GATAATTA others(12): Show |
1 | a0001c0003t0001g0234 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1629-55_1629-54ins others(19): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr15 | 40202530 | ||||||
chr15:40202751 | A | T | 193 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(190): Show |
229 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(226): Show |
intron_variant | MODIFIER | c.1734+57A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40202751 | |||||||
chr15:40202759 | A | C | 94 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(91): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.1734+65A>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40202759 | |||||||
chr15:40202866 | C | A | 109 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(106): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.1734+172C>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40202866 | |||||||
chr15:40202872 | A | G | 1 | a0001c0003t0001g0083 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1734+178A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40202872 | |||||||
chr15:40202894 | A | C | 2 | a0001c0003t0001g0278 a0001c0003t0001g0279 |
2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1734+200A>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40202894 | |||||||
chr15:40202903 | G | A | 1 | a0008c0011t0001g0276 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1734+209G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40202903 | |||||||
chr15:40203162 | A | G | 1 | a0002c0001t0002g0196 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1734+468A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40203162 | |||||||
chr15:40203313 | C | T | 141 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(138): Show |
171 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1734+619C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40203313 | |||||||
chr15:40203337 | T | TA | 32 | a0003c0005t0003g0008 a0003c0005t0003g0016 a0003c0005t0003g0113 others(29): Show |
38 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.1734+644dupA | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr15 | 40203337 | ||||||
chr15:40203563 | G | C | 11 | a0001c0004t0001g0003 a0001c0004t0001g0129 a0001c0004t0001g0130 others(8): Show |
15 | HG01109.hp1 HG02257.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.1734+869G>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40203563 | |||||||
chr15:40203798 | T | C | 1 | a0002c0001t0002g0183 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1734+1104T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40203798 | |||||||
chr15:40203921 | A | C | 109 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(106): Show |
136 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(133): Show |
intron_variant | MODIFIER | c.1734+1227A>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40203921 | |||||||
chr15:40203970 | C | T | 1 | a0001c0003t0001g0089 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1734+1276C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40203970 | |||||||
chr15:40204041 | A | G | 1 | a0002c0001t0002g0260 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1734+1347A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40204041 | |||||||
chr15:40204075 | T | A | 5 | a0001c0003t0001g0015 a0001c0003t0001g0079 a0001c0003t0001g0097 others(2): Show |
6 | NA18952.hp2 NA18965.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.1734+1381T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40204075 | |||||||
chr15:40204190 | T | C | 35 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0001g0149 others(32): Show |
40 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.1734+1496T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40204190 | |||||||
chr15:40204298 | A | G | 11 | a0003c0005t0003g0008 a0003c0005t0003g0113 a0003c0005t0003g0120 others(8): Show |
13 | HG00642.hp2 HG02055.hp2 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1734+1604A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40204298 | |||||||
chr15:40204440 | C | CT | 129 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(126): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(156): Show |
intron_variant | MODIFIER | c.1735-1731dupT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr15 | 40204440 | ||||||
chr15:40204440 | CT | C | 19 | a0001c0004t0001g0024 a0001c0004t0001g0236 a0001c0004t0001g0281 others(16): Show |
20 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(17): Show |
intron_variant | MODIFIER | c.1735-1731delT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr15 | 40204440 | ||||||
chr15:40204635 | A | T | 3 | a0002c0001t0002g0023 a0002c0001t0002g0247 a0002c0001t0002g0273 |
4 | HG00544.hp2 HG00621.hp1 NA18987.hp2 others(1): Show |
intron_variant | MODIFIER | c.1735-1549A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40204635 | |||||||
chr15:40204795 | C | A | 94 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(91): Show |
118 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.1735-1389C>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40204795 | |||||||
chr15:40204801 | T | C | 3 | a0001c0004t0001g0281 a0001c0004t0001g0288 a0001c0004t0001g0291 |
3 | HG01516.hp2 HG01517.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1735-1383T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40204801 | |||||||
chr15:40204894 | C | G | 1 | a0003c0020t0003g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1735-1290C>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40204894 | |||||||
chr15:40204944 | CT | C | 168 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(165): Show |
202 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(199): Show |
intron_variant | MODIFIER | c.1735-1220delT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr15 | 40204944 | ||||||
chr15:40205071 | C | T | 1 | a0002c0001t0002g0171 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1735-1113C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40205071 | |||||||
chr15:40205105 | C | T | 4 | a0001c0003t0001g0158 a0001c0003t0001g0159 a0001c0003t0001g0161 others(1): Show |
4 | NA18940.hp1 NA18983.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.1735-1079C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40205105 | |||||||
chr15:40205136 | G | A | 2 | a0001c0002t0001g0076 a0001c0002t0001g0107 |
2 | HG03490.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.1735-1048G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40205136 | |||||||
chr15:40205226 | C | T | 4 | a0001c0002t0001g0076 a0001c0002t0001g0107 a0004c0006t0001g0031 others(1): Show |
4 | HG03098.hp2 HG03490.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.1735-958C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40205226 | |||||||
chr15:40205242 | C | T | 1 | a0002c0001t0002g0166 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1735-942C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40205242 | |||||||
chr15:40205625 | C | T | 1 | a0001c0003t0001g0088 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1735-559C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40205625 | |||||||
chr15:40205688 | G | T | 5 | a0004c0006t0002g0153 a0004c0006t0002g0154 a0004c0006t0002g0155 others(2): Show |
5 | HG00741.hp2 HG02258.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1735-496G>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40205688 | |||||||
chr15:40205803 | G | A | 176 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(173): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.1735-381G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40205803 | |||||||
chr15:40205942 | A | G | 3 | a0001c0004t0001g0281 a0001c0004t0001g0288 a0001c0004t0001g0291 |
3 | HG01516.hp2 HG01517.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1735-242A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40205942 | |||||||
chr15:40205971 | T | C | 26 | a0003c0005t0003g0008 a0003c0005t0003g0016 a0003c0005t0003g0113 others(23): Show |
29 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.1735-213T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 14/22 | chr15 | 40205971 | |||||||
chr15:40206623 | T | C | 2 | a0002c0001t0002g0197 a0002c0001t0002g0217 |
2 | HG00741.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.2009+165T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 15/22 | chr15 | 40206623 | |||||||
chr15:40206738 | C | T | 1 | a0001c0004t0001g0131 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2009+280C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 15/22 | chr15 | 40206738 | |||||||
chr15:40206739 | G | T | 1 | a0001c0002t0001g0100 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.2009+281G>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 15/22 | chr15 | 40206739 | |||||||
chr15:40206880 | G | A | 1 | a0002c0001t0002g0257 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2009+422G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 15/22 | chr15 | 40206880 | |||||||
chr15:40206956 | C | T | 26 | a0003c0005t0003g0008 a0003c0005t0003g0016 a0003c0005t0003g0113 others(23): Show |
29 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.2009+498C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 15/22 | chr15 | 40206956 | |||||||
chr15:40207153 | A | T | 32 | a0003c0005t0003g0008 a0003c0005t0003g0016 a0003c0005t0003g0113 others(29): Show |
38 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2009+695A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 15/22 | chr15 | 40207153 | |||||||
chr15:40207569 | G | A | 1 | a0001c0002t0001g0075 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2010-1068G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 15/22 | chr15 | 40207569 | |||||||
chr15:40207675 | A | G | 1 | a0001c0003t0001g0079 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.2010-962A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 15/22 | chr15 | 40207675 | |||||||
chr15:40207697 | A | G | 2 | a0001c0003t0001g0151 a0001c0003t0001g0152 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2010-940A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 15/22 | chr15 | 40207697 | |||||||
chr15:40207880 | TA | T | 181 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(178): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.2010-745delA | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr15 | 40207880 | ||||||
chr15:40208041 | G | A | 1 | a0002c0001t0001g0253 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2010-596G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 15/22 | chr15 | 40208041 | |||||||
chr15:40208137 | TA | T | 32 | a0003c0005t0003g0008 a0003c0005t0003g0016 a0003c0005t0003g0113 others(29): Show |
38 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2010-488delA | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 15/22 | INFO_REALIGN_3_PRIME | chr15 | 40208137 | ||||||
chr15:40208224 | A | T | 32 | a0003c0005t0003g0008 a0003c0005t0003g0016 a0003c0005t0003g0113 others(29): Show |
38 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2010-413A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 15/22 | chr15 | 40208224 | |||||||
chr15:40208345 | C | T | 1 | a0001c0004t0001g0290 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2010-292C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 15/22 | chr15 | 40208345 | |||||||
chr15:40208390 | C | T | 176 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(173): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.2010-247C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 15/22 | chr15 | 40208390 | |||||||
chr15:40208468 | G | A | 1 | a0001c0002t0001g0163 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2010-169G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 15/22 | chr15 | 40208468 | |||||||
chr15:40208785 | C | T | 109 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(106): Show |
133 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(130): Show |
intron_variant | MODIFIER | c.2143+15C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 16/22 | chr15 | 40208785 | |||||||
chr15:40209006 | G | A | 1 | a0002c0001t0002g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2143+236G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 16/22 | chr15 | 40209006 | |||||||
chr15:40209107 | C | T | 6 | a0001c0003t0001g0028 a0001c0003t0001g0085 a0001c0003t0001g0086 others(3): Show |
6 | HG00099.hp1 HG01069.hp2 HG01123.hp1 others(3): Show |
intron_variant | MODIFIER | c.2143+337C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 16/22 | chr15 | 40209107 | |||||||
chr15:40209216 | C | T | 1 | a0001c0003t0001g0025 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2144-419C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 16/22 | chr15 | 40209216 | |||||||
chr15:40209277 | C | T | 32 | a0003c0005t0003g0008 a0003c0005t0003g0016 a0003c0005t0003g0113 others(29): Show |
38 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2144-358C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 16/22 | chr15 | 40209277 | |||||||
chr15:40209300 | A | C | 1 | a0001c0003t0001g0224 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2144-335A>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 16/22 | chr15 | 40209300 | |||||||
chr15:40209419 | G | A | 2 | a0001c0003t0001g0151 a0001c0003t0001g0152 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2144-216G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 16/22 | chr15 | 40209419 | |||||||
chr15:40209544 | AT | A | 32 | a0003c0005t0003g0008 a0003c0005t0003g0016 a0003c0005t0003g0113 others(29): Show |
38 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2144-81delT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr15 | 40209544 | ||||||
chr15:40209792 | T | G | 32 | a0003c0005t0003g0008 a0003c0005t0003g0016 a0003c0005t0003g0113 others(29): Show |
38 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2284+17T>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 17/22 | chr15 | 40209792 | |||||||
chr15:40209888 | A | T | 1 | a0002c0001t0002g0246 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2284+113A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 17/22 | chr15 | 40209888 | |||||||
chr15:40210659 | G | A | 2 | a0001c0003t0001g0231 a0001c0003t0001g0233 |
2 | NA18965.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.2385+449G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 18/22 | chr15 | 40210659 | |||||||
chr15:40210693 | C | T | 1 | a0001c0002t0001g0058 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2385+483C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 18/22 | chr15 | 40210693 | |||||||
chr15:40210708 | G | A | 1 | a0002c0001t0002g0239 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2385+498G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 18/22 | chr15 | 40210708 | |||||||
chr15:40211025 | C | T | 1 | a0002c0001t0002g0187 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2385+815C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 18/22 | chr15 | 40211025 | |||||||
chr15:40211140 | T | C | 1 | a0002c0001t0001g0164 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2385+930T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 18/22 | chr15 | 40211140 | |||||||
chr15:40211338 | C | T | 26 | a0003c0005t0003g0008 a0003c0005t0003g0016 a0003c0005t0003g0113 others(23): Show |
29 | HG00642.hp2 HG02055.hp1 HG02055.hp2 others(26): Show |
intron_variant | MODIFIER | c.2385+1128C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 18/22 | chr15 | 40211338 | |||||||
chr15:40211511 | T | A | 3 | a0001c0003t0001g0028 a0001c0003t0001g0086 a0001c0003t0001g0089 |
3 | HG00099.hp1 HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.2386-988T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 18/22 | chr15 | 40211511 | |||||||
chr15:40211538 | T | G | 1 | a0001c0002t0001g0063 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.2386-961T>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 18/22 | chr15 | 40211538 | |||||||
chr15:40211624 | T | A | 4 | a0001c0003t0001g0158 a0001c0003t0001g0159 a0001c0003t0001g0161 others(1): Show |
4 | NA18940.hp1 NA18983.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.2386-875T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 18/22 | chr15 | 40211624 | |||||||
chr15:40211679 | G | A | 1 | a0003c0005t0003g0121 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2386-820G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 18/22 | chr15 | 40211679 | |||||||
chr15:40211684 | G | C | 4 | a0001c0003t0001g0158 a0001c0003t0001g0159 a0001c0003t0001g0161 others(1): Show |
4 | NA18940.hp1 NA18983.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.2386-815G>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 18/22 | chr15 | 40211684 | |||||||
chr15:40211824 | G | GT | 21 | a0001c0003t0001g0149 a0001c0004t0001g0024 a0001c0004t0001g0236 others(18): Show |
22 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.2386-664dupT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr15 | 40211824 | ||||||
chr15:40211831 | T | G | 1 | a0002c0001t0002g0201 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2386-668T>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 18/22 | chr15 | 40211831 | |||||||
chr15:40211936 | T | C | 160 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(157): Show |
191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.2386-563T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 18/22 | chr15 | 40211936 | |||||||
chr15:40211948 | G | A | 1 | a0002c0001t0002g0305 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.2386-551G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 18/22 | chr15 | 40211948 | |||||||
chr15:40212135 | T | C | 1 | a0002c0001t0002g0184 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2386-364T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 18/22 | chr15 | 40212135 | |||||||
chr15:40212311 | C | G | 5 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0001g0149 others(2): Show |
5 | HG02145.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2386-188C>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 18/22 | chr15 | 40212311 | |||||||
chr15:40212311 | C | T | 1 | a0002c0001t0002g0169 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2386-188C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 18/22 | chr15 | 40212311 | |||||||
chr15:40212793 | C | T | 1 | a0001c0004t0001g0165 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2535+145C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 19/22 | chr15 | 40212793 | |||||||
chr15:40212843 | C | T | 1 | a0002c0001t0002g0248 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2535+195C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 19/22 | chr15 | 40212843 | |||||||
chr15:40212877 | A | G | 32 | a0003c0005t0003g0008 a0003c0005t0003g0016 a0003c0005t0003g0113 others(29): Show |
38 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2535+229A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 19/22 | chr15 | 40212877 | |||||||
chr15:40212945 | C | T | 2 | a0004c0006t0001g0031 a0004c0006t0001g0034 |
2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2535+297C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 19/22 | chr15 | 40212945 | |||||||
chr15:40212981 | T | C | 1 | a0002c0001t0002g0266 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2535+333T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 19/22 | chr15 | 40212981 | |||||||
chr15:40212992 | T | A | 1 | a0008c0011t0001g0276 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2536-340T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 19/22 | chr15 | 40212992 | |||||||
chr15:40213030 | G | C | 5 | a0003c0005t0003g0016 a0003c0005t0003g0139 a0003c0005t0003g0140 others(2): Show |
6 | HG02280.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.2536-302G>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 19/22 | chr15 | 40213030 | |||||||
chr15:40213077 | AT | A | 32 | a0003c0005t0003g0008 a0003c0005t0003g0016 a0003c0005t0003g0113 others(29): Show |
38 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2536-254delT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 19/22 | chr15 | 40213077 | |||||||
chr15:40213079 | C | A | 32 | a0003c0005t0003g0008 a0003c0005t0003g0016 a0003c0005t0003g0113 others(29): Show |
38 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2536-253C>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 19/22 | chr15 | 40213079 | |||||||
chr15:40213218 | T | C | 9 | a0004c0006t0001g0031 a0004c0006t0001g0032 a0004c0006t0001g0033 others(6): Show |
9 | HG00741.hp2 HG02258.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.2536-114T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 19/22 | chr15 | 40213218 | |||||||
chr15:40213221 | G | A | 2 | a0001c0003t0001g0159 a0001c0003t0006g0160 |
2 | NA18983.hp2 NA19089.hp1 |
intron_variant | MODIFIER | c.2536-111G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 19/22 | chr15 | 40213221 | |||||||
chr15:40213228 | T | C | 127 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(124): Show |
152 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(149): Show |
intron_variant | MODIFIER | c.2536-104T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 19/22 | chr15 | 40213228 | |||||||
chr15:40213649 | T | A | 2 | a0002c0001t0002g0173 a0002c0001t0002g0191 |
2 | HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.2678+175T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40213649 | |||||||
chr15:40213660 | C | CTAG | 32 | a0003c0005t0003g0008 a0003c0005t0003g0016 a0003c0005t0003g0113 others(29): Show |
38 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2678+190_2678+192d others(5): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr15 | 40213660 | ||||||
chr15:40213887 | A | G | 1 | a0001c0003t0001g0109 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2678+413A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40213887 | |||||||
chr15:40214057 | G | T | 1 | a0001c0002t0001g0055 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2678+583G>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40214057 | |||||||
chr15:40214126 | A | T | 1 | a0008c0011t0001g0276 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.2678+652A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40214126 | |||||||
chr15:40214230 | C | T | 32 | a0003c0005t0003g0008 a0003c0005t0003g0016 a0003c0005t0003g0113 others(29): Show |
38 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2678+756C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40214230 | |||||||
chr15:40214298 | C | T | 4 | a0003c0005t0003g0114 a0003c0005t0003g0115 a0003c0005t0003g0116 others(1): Show |
4 | HG02055.hp1 HG03130.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2678+824C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40214298 | |||||||
chr15:40214429 | T | C | 1 | a0002c0001t0002g0169 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2678+955T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40214429 | |||||||
chr15:40214694 | C | T | 7 | a0001c0002t0001g0001 a0001c0002t0001g0052 a0001c0002t0001g0056 others(4): Show |
9 | HG00597.hp2 HG00609.hp1 HG02083.hp2 others(6): Show |
intron_variant | MODIFIER | c.2678+1220C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40214694 | |||||||
chr15:40214695 | C | T | 1 | a0001c0002t0001g0042 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.2678+1221C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40214695 | |||||||
chr15:40214810 | T | C | 1 | a0001c0004t0001g0282 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2678+1336T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40214810 | |||||||
chr15:40214833 | TC | T | 7 | a0001c0003t0001g0158 a0001c0003t0001g0159 a0001c0003t0001g0161 others(4): Show |
7 | NA18940.hp1 NA18983.hp2 NA19009.hp1 others(4): Show |
intron_variant | MODIFIER | c.2678+1366delC | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr15 | 40214833 | ||||||
chr15:40214848 | C | A | 1 | a0004c0006t0002g0157 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2678+1374C>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40214848 | |||||||
chr15:40215042 | T | G | 34 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0001g0149 others(31): Show |
39 | HG00140.hp1 HG00735.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.2678+1568T>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40215042 | |||||||
chr15:40215160 | A | AT | 32 | a0003c0005t0003g0008 a0003c0005t0003g0016 a0003c0005t0003g0113 others(29): Show |
38 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2678+1688dupT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr15 | 40215160 | ||||||
chr15:40215212 | A | T | 1 | a0002c0001t0002g0211 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2678+1738A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40215212 | |||||||
chr15:40215279 | G | C | 111 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(108): Show |
135 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(132): Show |
intron_variant | MODIFIER | c.2678+1805G>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40215279 | |||||||
chr15:40215341 | G | A | 1 | a0002c0001t0002g0196 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2678+1867G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40215341 | |||||||
chr15:40215496 | G | A | 5 | a0001c0002t0001g0076 a0001c0003t0001g0158 a0001c0003t0001g0159 others(2): Show |
5 | HG04204.hp1 NA18940.hp1 NA18983.hp2 others(2): Show |
intron_variant | MODIFIER | c.2679-2000G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40215496 | |||||||
chr15:40215630 | G | A | 32 | a0003c0005t0003g0008 a0003c0005t0003g0016 a0003c0005t0003g0113 others(29): Show |
38 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.2679-1866G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40215630 | |||||||
chr15:40215643 | C | T | 1 | a0001c0003t0001g0025 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2679-1853C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40215643 | |||||||
chr15:40215886 | C | T | 11 | a0001c0004t0001g0003 a0001c0004t0001g0129 a0001c0004t0001g0130 others(8): Show |
15 | HG01109.hp1 HG02257.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.2679-1610C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40215886 | |||||||
chr15:40216123 | A | C | 110 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(107): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.2679-1373A>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216123 | |||||||
chr15:40216129 | C | T | 1 | a0001c0002t0001g0043 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2679-1367C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216129 | |||||||
chr15:40216238 | G | C | 110 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(107): Show |
134 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(131): Show |
intron_variant | MODIFIER | c.2679-1258G>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216238 | |||||||
chr15:40216392 | C | T | 1 | a0001c0002t0001g0107 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.2679-1104C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216392 | |||||||
chr15:40216544 | A | G | 1 | a0003c0020t0003g0112 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2679-952A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216544 | |||||||
chr15:40216547 | C | CTA | 3 | a0001c0003t0001g0158 a0001c0003t0001g0161 a0002c0001t0002g0211 |
3 | NA18940.hp1 NA19011.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2679-925_2679-924d others(4): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr15 | 40216547 | ||||||
chr15:40216547 | CTA | C | 86 | a0001c0002t0001g0010 a0001c0002t0001g0036 a0001c0002t0001g0037 others(83): Show |
99 | HG00280.hp2 HG00408.hp2 HG00544.hp1 others(96): Show |
intron_variant | MODIFIER | c.2679-925_2679-924d others(4): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr15 | 40216547 | ||||||
chr15:40216547 | CTATA | C | 15 | a0001c0003t0001g0012 a0001c0003t0001g0027 a0001c0004t0001g0281 others(12): Show |
16 | HG01516.hp2 HG01517.hp1 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.2679-927_2679-924d others(6): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr15 | 40216547 | ||||||
chr15:40216547 | CTATATA | C | 3 | a0001c0002t0001g0054 a0001c0004t0001g0285 a0011c0010t0001g0277 |
3 | HG00735.hp2 HG03041.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.2679-929_2679-924d others(8): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr15 | 40216547 | ||||||
chr15:40216559 | ATATATAT others(8): Show |
A | 2 | a0003c0005t0003g0115 a0003c0005t0003g0117 |
2 | HG03130.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.2679-935_2679-921d others(17): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr15 | 40216559 | ||||||
chr15:40216561 | ATATATAT others(7): Show |
A | 1 | a0003c0005t0003g0140 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2679-933_2679-920d others(16): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr15 | 40216561 | ||||||
chr15:40216561 | ATATATAT others(8): Show |
A | 3 | a0003c0005t0003g0144 a0003c0020t0003g0112 a0005c0007t0003g0005 |
3 | HG02615.hp2 HG02647.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2679-933_2679-919d others(17): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr15 | 40216561 | ||||||
chr15:40216561 | ATATATAT others(9): Show |
A | 3 | a0003c0005t0003g0016 a0003c0005t0003g0141 a0009c0018t0003g0142 |
4 | HG02280.hp1 HG02622.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2679-933_2679-918d others(18): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr15 | 40216561 | ||||||
chr15:40216563 | ATATATAT others(7): Show |
A | 1 | a0003c0005t0003g0139 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2679-931_2679-918d others(16): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr15 | 40216563 | ||||||
chr15:40216563 | ATATATAT others(8): Show |
A | 24 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0113 others(21): Show |
28 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.2679-931_2679-917d others(17): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr15 | 40216563 | ||||||
chr15:40216564 | TA | T | 3 | a0001c0002t0001g0026 a0001c0003t0001g0025 a0001c0003t0001g0225 |
3 | HG02486.hp2 NA18954.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2679-931delA | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216564 | |||||||
chr15:40216564 | TATA | T | 4 | a0001c0003t0001g0088 a0002c0001t0002g0191 a0002c0001t0002g0262 others(1): Show |
4 | HG01123.hp1 HG03139.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.2679-931_2679-929d others(5): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216564 | |||||||
chr15:40216566 | TA | T | 30 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(27): Show |
41 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.2679-929delA | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216566 | |||||||
chr15:40216566 | TATA | T | 36 | a0001c0003t0001g0014 a0001c0003t0001g0028 a0001c0003t0001g0070 others(33): Show |
37 | HG00099.hp1 HG00544.hp2 HG00597.hp1 others(34): Show |
intron_variant | MODIFIER | c.2679-929_2679-927d others(5): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216566 | |||||||
chr15:40216567 | A | T | 5 | a0001c0002t0001g0001 a0001c0002t0001g0026 a0001c0002t0001g0047 others(2): Show |
5 | HG02486.hp2 HG03704.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.2679-929A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216567 | |||||||
chr15:40216568 | TA | T | 13 | a0001c0002t0001g0030 a0001c0002t0001g0046 a0001c0002t0001g0064 others(10): Show |
14 | HG01255.hp1 HG01361.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.2679-927delA | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216568 | |||||||
chr15:40216568 | TATA | T | 27 | a0001c0003t0001g0013 a0001c0003t0001g0039 a0001c0003t0001g0084 others(24): Show |
32 | HG01496.hp2 HG02004.hp2 HG02257.hp2 others(29): Show |
intron_variant | MODIFIER | c.2679-927_2679-925d others(5): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216568 | |||||||
chr15:40216569 | A | T | 65 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(62): Show |
79 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.2679-927A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216569 | |||||||
chr15:40216570 | TA | T | 12 | a0001c0002t0001g0163 a0001c0003t0001g0009 a0001c0003t0001g0045 others(9): Show |
13 | HG01175.hp1 HG01978.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.2679-925delA | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216570 | |||||||
chr15:40216571 | A | T | 177 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(174): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.2679-925A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216571 | |||||||
chr15:40216571 | ATTTT | A | 8 | a0001c0004t0001g0236 a0001c0004t0001g0282 a0001c0004t0001g0283 others(5): Show |
8 | HG00735.hp1 HG01884.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.2679-913_2679-910d others(6): Show |
BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr15 | 40216571 | ||||||
chr15:40216573 | T | A | 5 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0001c0003t0001g0158 others(2): Show |
5 | HG02647.hp2 HG02717.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2679-923T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216573 | |||||||
chr15:40216574 | T | A | 1 | a0004c0006t0002g0153 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2679-922T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216574 | |||||||
chr15:40216575 | T | A | 4 | a0001c0003t0001g0151 a0001c0003t0001g0152 a0001c0003t0001g0158 others(1): Show |
4 | HG00741.hp2 HG02717.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2679-921T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216575 | |||||||
chr15:40216577 | T | A | 2 | a0001c0003t0001g0151 a0001c0004t0001g0293 |
2 | HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2679-919T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216577 | |||||||
chr15:40216586 | T | A | 18 | a0002c0001t0002g0022 a0002c0001t0002g0241 a0002c0001t0002g0254 others(15): Show |
22 | HG00673.hp2 HG01081.hp1 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.2679-910T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216586 | |||||||
chr15:40216701 | A | G | 4 | a0002c0001t0002g0017 a0002c0001t0002g0195 a0002c0001t0002g0197 others(1): Show |
5 | HG00280.hp2 HG00741.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.2679-795A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216701 | |||||||
chr15:40216815 | A | G | 1 | a0002c0001t0002g0175 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.2679-681A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216815 | |||||||
chr15:40216873 | A | T | 3 | a0001c0002t0001g0037 a0001c0002t0001g0099 a0001c0002t0001g0162 |
3 | HG00099.hp2 HG01361.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.2679-623A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216873 | |||||||
chr15:40216989 | C | A | 1 | a0010c0012t0001g0280 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2679-507C>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40216989 | |||||||
chr15:40217104 | G | A | 1 | a0003c0005t0003g0145 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2679-392G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40217104 | |||||||
chr15:40217132 | T | A | 1 | a0001c0004t0001g0286 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2679-364T>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40217132 | |||||||
chr15:40217320 | A | G | 4 | a0001c0003t0001g0158 a0001c0003t0001g0159 a0001c0003t0001g0161 others(1): Show |
4 | NA18940.hp1 NA18983.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.2679-176A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40217320 | |||||||
chr15:40217399 | A | G | 95 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(92): Show |
119 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.2679-97A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | chr15 | 40217399 | |||||||
chr15:40217417 | C | CT | 17 | a0001c0003t0001g0021 a0001c0003t0001g0168 a0001c0003t0001g0224 others(14): Show |
18 | HG01168.hp1 HG01169.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.2679-69dupT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr15 | 40217417 | ||||||
chr15:40217775 | A | G | 3 | a0001c0004t0001g0130 a0008c0011t0001g0276 a0011c0010t0001g0277 |
3 | HG02451.hp2 HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2850+108A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 21/22 | chr15 | 40217775 | |||||||
chr15:40217842 | A | C | 1 | a0001c0003t0001g0082 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.2850+175A>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 21/22 | chr15 | 40217842 | |||||||
chr15:40217855 | T | C | 51 | a0001c0004t0001g0024 a0001c0004t0001g0236 a0001c0004t0001g0281 others(48): Show |
58 | HG00140.hp1 HG00642.hp2 HG00735.hp1 others(55): Show |
intron_variant | MODIFIER | c.2850+188T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 21/22 | chr15 | 40217855 | |||||||
chr15:40217883 | C | T | 2 | a0001c0003t0001g0151 a0001c0003t0001g0152 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2850+216C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 21/22 | chr15 | 40217883 | |||||||
chr15:40218115 | A | T | 4 | a0001c0003t0001g0147 a0001c0003t0001g0148 a0001c0003t0001g0149 others(1): Show |
4 | HG02145.hp1 HG02559.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.2851-341A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 21/22 | chr15 | 40218115 | |||||||
chr15:40218139 | A | G | 33 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(30): Show |
39 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.2851-317A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 21/22 | chr15 | 40218139 | |||||||
chr15:40218325 | A | G | 5 | a0001c0003t0001g0224 a0001c0003t0001g0225 a0001c0003t0001g0226 others(2): Show |
5 | HG01255.hp1 HG02486.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.2851-131A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 21/22 | chr15 | 40218325 | |||||||
chr15:40218915 | A | C | 2 | a0001c0003t0001g0151 a0001c0003t0001g0152 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2957+353A>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 22/22 | chr15 | 40218915 | |||||||
chr15:40218981 | G | A | 18 | a0001c0004t0001g0024 a0001c0004t0001g0236 a0001c0004t0001g0281 others(15): Show |
19 | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.2957+419G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 22/22 | chr15 | 40218981 | |||||||
chr15:40219153 | G | A | 1 | a0002c0001t0002g0240 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2957+591G>A | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 22/22 | chr15 | 40219153 | |||||||
chr15:40219229 | A | G | 33 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(30): Show |
39 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.2957+667A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 22/22 | chr15 | 40219229 | |||||||
chr15:40219498 | A | G | 1 | a0002c0001t0002g0256 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2957+936A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 22/22 | chr15 | 40219498 | |||||||
chr15:40219714 | C | T | 1 | a0002c0001t0002g0218 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2958-850C>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 22/22 | chr15 | 40219714 | |||||||
chr15:40219718 | T | C | 2 | a0001c0003t0001g0151 a0001c0003t0001g0152 |
2 | HG02717.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2958-846T>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 22/22 | chr15 | 40219718 | |||||||
chr15:40219728 | C | CT | 179 | a0001c0002t0001g0001 a0001c0002t0001g0006 a0001c0002t0001g0007 others(176): Show |
214 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(211): Show |
intron_variant | MODIFIER | c.2958-835dupT | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr15 | 40219728 | ||||||
chr15:40219985 | A | T | 1 | a0002c0001t0002g0172 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2958-579A>T | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 22/22 | chr15 | 40219985 | |||||||
chr15:40220142 | G | C | 33 | a0001c0019t0003g0143 a0003c0005t0003g0008 a0003c0005t0003g0016 others(30): Show |
39 | HG00642.hp2 HG01081.hp1 HG01243.hp1 others(36): Show |
intron_variant | MODIFIER | c.2958-422G>C | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 22/22 | chr15 | 40220142 | |||||||
chr15:40220223 | A | G | 2 | a0002c0001t0002g0171 a0002c0001t0002g0296 |
2 | NA18945.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.2958-341A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 22/22 | chr15 | 40220223 | |||||||
chr15:40220279 | A | G | 1 | a0002c0001t0002g0218 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2958-285A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 22/22 | chr15 | 40220279 | |||||||
chr15:40220430 | A | G | 10 | a0001c0004t0001g0003 a0001c0004t0001g0129 a0001c0004t0001g0130 others(7): Show |
14 | HG02257.hp2 HG02572.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.2958-134A>G | BUB1B | ENSG00000156970.13 | transcript | ENST00000287598.11 | protein_coding | 22/22 | chr15 | 40220430 |