Item | Value |
---|---|
geneid | 51667 |
ensemblid | ENSG00000013374.17 |
hgncid | 17623 |
symbol | NUB1 |
name | negative regulator of ubiquitin like proteins 1 |
refseq_nuc | NM_001243351.2 |
refseq_prot | NP_001230280.2 |
ensembl_nuc | ENST00000568733.6 |
ensembl_prot | ENSP00000454264.2 |
mane_status | MANE Select |
chr | chr7 |
start | 151341812 |
end | 151378449 |
strand | + |
ver | v1.2 |
region | chr7:151341812-151378449 |
region5000 | chr7:151336812-151383449 |
regionname0 | NUB1_chr7_151341812_151378449 |
regionname5000 | NUB1_chr7_151336812_151383449 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 615 | 406 | 94 | 76 | 169 | 16 | 49 | 132 | NUB1_chr7_151336812_151383449 | NUB1 | MAQKK others(610): Show |
chr7 | 151336812 | 151383449 |
a0002 | 0/0 | 615 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | MAQNK others(610): Show |
chr7 | 151336812 | 151383449 |
a0003 | 0/0 | 615 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | NUB1_chr7_151336812_151383449 | NUB1 | MAQKK others(610): Show |
chr7 | 151336812 | 151383449 |
a0004 | 0/0 | 615 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | MAQKK others(610): Show |
chr7 | 151336812 | 151383449 |
a0005 | 0/0 | 615 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | MAQKK others(610): Show |
chr7 | 151336812 | 151383449 |
a0006 | 0/0 | 615 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | MAQKK others(610): Show |
chr7 | 151336812 | 151383449 |
a0007 | 0/0 | 615 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | MAQKK others(610): Show |
chr7 | 151336812 | 151383449 |
a0008 | 0/0 | 615 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | MAQKK others(610): Show |
chr7 | 151336812 | 151383449 |
a0009 | 0/0 | 615 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | MAQKK others(610): Show |
chr7 | 151336812 | 151383449 |
a0010 | 0/0 | 615 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | MAQKK others(610): Show |
chr7 | 151336812 | 151383449 |
a0011 | 0/0 | 615 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | MAQKK others(610): Show |
chr7 | 151336812 | 151383449 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 1845 | 258 | 81 | 46 | 82 | 9 | 39 | NUB1_chr7_151336812_151383449 | NUB1 | ATGGC others(1840): Show |
chr7 | 151336812 | 151383449 | ||
a0001c0002 | 0/1 | 1845 | 120 | 8 | 25 | 73 | 5 | 8 | NUB1_chr7_151336812_151383449 | NUB1 | ATGGC others(1840): Show |
chr7 | 151336812 | 151383449 | ||
a0001c0003 | 0/0 | 1845 | 15 | 3 | 4 | 5 | 2 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | ATGGC others(1840): Show |
chr7 | 151336812 | 151383449 | ||
a0001c0004 | 0/0 | 1845 | 11 | 0 | 1 | 9 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | ATGGC others(1840): Show |
chr7 | 151336812 | 151383449 | ||
a0001c0005 | 0/0 | 1845 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ATGGC others(1840): Show |
chr7 | 151336812 | 151383449 | ||
a0002c0007 | 0/0 | 1845 | 2 | 0 | 2 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ATGGC others(1840): Show |
chr7 | 151336812 | 151383449 | ||
a0003c0006 | 0/0 | 1845 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ATGGC others(1840): Show |
chr7 | 151336812 | 151383449 | ||
a0004c0015 | 0/0 | 1845 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ATGGC others(1840): Show |
chr7 | 151336812 | 151383449 | ||
a0005c0010 | 0/0 | 1845 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ATGGC others(1840): Show |
chr7 | 151336812 | 151383449 | ||
a0006c0011 | 0/0 | 1845 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ATGGC others(1840): Show |
chr7 | 151336812 | 151383449 | ||
a0007c0012 | 0/0 | 1845 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | ATGGC others(1840): Show |
chr7 | 151336812 | 151383449 | ||
a0008c0014 | 0/0 | 1845 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ATGGC others(1840): Show |
chr7 | 151336812 | 151383449 | ||
a0009c0008 | 0/0 | 1845 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ATGGC others(1840): Show |
chr7 | 151336812 | 151383449 | ||
a0010c0013 | 0/0 | 1845 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ATGGC others(1840): Show |
chr7 | 151336812 | 151383449 | ||
a0011c0009 | 0/0 | 1845 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ATGGC others(1840): Show |
chr7 | 151336812 | 151383449 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3109 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0001c0001t0002 | 0/0 | 3109 | 92 | 10 | 27 | 53 | 1 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0001c0001t0003 | 1/0 | 3109 | 67 | 28 | 12 | 0 | 6 | 20 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0001c0001t0004 | 0/0 | 3109 | 55 | 24 | 4 | 15 | 1 | 11 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0001c0001t0005 | 0/0 | 3109 | 22 | 0 | 2 | 13 | 1 | 6 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0001c0001t0006 | 0/0 | 3109 | 10 | 10 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0001c0001t0007 | 0/0 | 3109 | 6 | 6 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0001c0001t0008 | 0/0 | 3109 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0001c0001t0010 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0001c0001t0011 | 0/0 | 3109 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0001c0001t0012 | 0/0 | 3109 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0001c0002t0001 | 0/1 | 3109 | 119 | 8 | 25 | 73 | 5 | 7 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0001c0002t0013 | 0/0 | 3109 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0001c0003t0002 | 0/0 | 3109 | 8 | 0 | 4 | 3 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0001c0003t0003 | 0/0 | 3109 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0001c0003t0004 | 0/0 | 3109 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0001c0003t0005 | 0/0 | 3109 | 2 | 0 | 0 | 0 | 1 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0001c0003t0007 | 0/0 | 3109 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0001c0004t0001 | 0/0 | 3109 | 11 | 0 | 1 | 9 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0001c0005t0001 | 0/0 | 3109 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0002c0007t0004 | 0/0 | 3109 | 2 | 0 | 2 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0003c0006t0002 | 0/0 | 3109 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0004c0015t0002 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0005c0010t0003 | 0/0 | 3109 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0006c0011t0003 | 0/0 | 3109 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0007c0012t0003 | 0/0 | 3109 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0008c0014t0001 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0009c0008t0009 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0010c0013t0001 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
a0011c0009t0009 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | ACTCT others(3104): Show |
chr7 | 151336812 | 151383449 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0001 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0003 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0005 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0002g0371 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0027 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0346 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0348 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0351 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0355 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0357 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0359 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0361 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0362 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0367 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0003g0374 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0007 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0024 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0347 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0352 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0354 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0370 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0004g0373 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0363 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0366 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0369 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0005g0372 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0006g0008 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0006g0009 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0006g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0006g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0006g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0007g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0007g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0007g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0007g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0008g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0008g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0010g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0011g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0001t0012g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0300 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0001g0376 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0002t0013g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0002g0306 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0002g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0002g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0002g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0003g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0004g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0004g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0005g0308 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0005g0364 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0003t0007g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0004t0001g0358 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0005t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0001c0005t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0002c0007t0004g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0002c0007t0004g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0003c0006t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0003c0006t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0004c0015t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0005c0010t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0006c0011t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0007c0012t0003g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0008c0014t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0009c0008t0009g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0010c0013t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
a0011c0009t0009g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0352 | EUR | GBR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0339 | EUR | GBR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0362 | EUR | GBR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00140 | hp2 | a0001 | c0003 | t0002 | g0306 | EUR | GBR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00280 | hp1 | a0001 | c0001 | t0003 | g0346 | EUR | FIN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00280 | hp2 | a0001 | c0001 | t0005 | g0108 | EUR | FIN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00323 | hp1 | a0001 | c0003 | t0005 | g0308 | EUR | FIN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0282 | EUR | FIN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00408 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00423 | hp1 | a0001 | c0001 | t0004 | g0079 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00423 | hp2 | a0001 | c0003 | t0002 | g0243 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0080 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00438 | hp2 | a0001 | c0001 | t0004 | g0217 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00597 | hp2 | a0001 | c0001 | t0005 | g0321 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00609 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00621 | hp1 | a0001 | c0003 | t0004 | g0190 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00639 | hp1 | a0001 | c0002 | t0001 | g0153 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0342 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0332 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0228 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0224 | EAS | CHS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0263 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0270 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00738 | hp1 | a0001 | c0002 | t0001 | g0310 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00738 | hp2 | a0001 | c0001 | t0003 | g0367 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00741 | hp1 | a0001 | c0002 | t0001 | g0302 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG00741 | hp2 | a0001 | c0002 | t0001 | g0165 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01070 | hp2 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01071 | hp1 | a0001 | c0002 | t0001 | g0031 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01074 | hp1 | a0002 | c0007 | t0004 | g0312 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0350 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0356 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0338 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01106 | hp1 | a0001 | c0001 | t0012 | g0285 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0314 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01109 | hp1 | a0001 | c0003 | t0002 | g0036 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01167 | hp1 | a0001 | c0003 | t0002 | g0328 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01168 | hp1 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0374 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0025 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0030 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0106 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0140 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01243 | hp2 | a0002 | c0007 | t0004 | g0303 | AMR | PUR | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0258 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01256 | hp2 | a0001 | c0003 | t0002 | g0334 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0137 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01257 | hp2 | a0001 | c0002 | t0001 | g0289 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01258 | hp1 | a0001 | c0003 | t0002 | g0335 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01258 | hp2 | a0001 | c0002 | t0001 | g0290 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01261 | hp1 | a0001 | c0001 | t0003 | g0027 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0055 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01346 | hp1 | a0001 | c0002 | t0001 | g0301 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01346 | hp2 | a0001 | c0002 | t0001 | g0148 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0322 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01358 | hp2 | a0001 | c0001 | t0005 | g0363 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01361 | hp1 | a0001 | c0001 | t0005 | g0372 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0351 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0234 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01496 | hp2 | a0001 | c0004 | t0001 | g0175 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01515 | hp1 | a0001 | c0002 | t0001 | g0325 | EUR | IBS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0278 | EUR | IBS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01517 | hp1 | a0001 | c0002 | t0001 | g0340 | EUR | IBS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01517 | hp2 | a0001 | c0001 | t0003 | g0023 | EUR | IBS | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0210 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0269 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01891 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0317 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0098 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0283 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01934 | hp2 | a0001 | c0002 | t0001 | g0075 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0266 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01975 | hp1 | a0001 | c0002 | t0001 | g0166 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0353 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02015 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02015 | hp2 | a0001 | c0001 | t0004 | g0247 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0146 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02027 | hp2 | a0004 | c0015 | t0002 | g0125 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02040 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02055 | hp2 | a0005 | c0010 | t0003 | g0209 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02056 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02071 | hp1 | a0001 | c0002 | t0001 | g0246 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0249 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02074 | hp1 | a0001 | c0001 | t0004 | g0333 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02074 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02080 | hp1 | a0001 | c0003 | t0002 | g0105 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02132 | hp1 | a0001 | c0002 | t0001 | g0236 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02135 | hp1 | a0001 | c0004 | t0001 | g0101 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02135 | hp2 | a0001 | c0002 | t0001 | g0141 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0152 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0273 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0035 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02155 | hp1 | a0001 | c0002 | t0001 | g0255 | EAS | CDX | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02155 | hp2 | a0001 | c0002 | t0001 | g0104 | EAS | CDX | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0365 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02257 | hp2 | a0006 | c0011 | t0003 | g0189 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0370 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02258 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02280 | hp1 | a0001 | c0001 | t0004 | g0211 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02280 | hp2 | a0001 | c0001 | t0003 | g0326 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02300 | hp1 | a0001 | c0002 | t0001 | g0368 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02451 | hp1 | a0001 | c0002 | t0001 | g0262 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0265 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02523 | hp1 | a0001 | c0001 | t0004 | g0239 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0119 | EAS | KHV | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02572 | hp1 | a0001 | c0001 | t0007 | g0186 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0313 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0357 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0109 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0180 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02622 | hp1 | a0001 | c0001 | t0007 | g0145 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0259 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02630 | hp1 | a0001 | c0001 | t0003 | g0320 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0288 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02647 | hp1 | a0001 | c0001 | t0008 | g0203 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0034 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0355 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02683 | hp2 | a0001 | c0002 | t0013 | g0284 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0371 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02698 | hp2 | a0007 | c0012 | t0003 | g0163 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0037 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02717 | hp2 | a0001 | c0001 | t0007 | g0107 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0181 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02735 | hp1 | a0001 | c0001 | t0003 | g0331 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02735 | hp2 | a0001 | c0001 | t0005 | g0323 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0347 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02738 | hp2 | a0001 | c0001 | t0003 | g0150 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02809 | hp1 | a0001 | c0001 | t0006 | g0305 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0212 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0033 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0132 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0135 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0316 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0026 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02896 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02897 | hp1 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02897 | hp2 | a0001 | c0001 | t0006 | g0026 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0360 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02922 | hp2 | a0001 | c0001 | t0007 | g0256 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02965 | hp1 | a0001 | c0001 | t0004 | g0187 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0039 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0007 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03017 | hp1 | a0001 | c0002 | t0001 | g0160 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03017 | hp2 | a0001 | c0001 | t0003 | g0157 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03041 | hp1 | a0001 | c0001 | t0004 | g0324 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03041 | hp2 | a0001 | c0001 | t0003 | g0277 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0179 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0274 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0261 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03139 | hp1 | a0001 | c0001 | t0007 | g0183 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0275 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0373 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03239 | hp1 | a0001 | c0001 | t0005 | g0369 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0348 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0319 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03453 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0040 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03490 | hp2 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03491 | hp1 | a0001 | c0001 | t0004 | g0159 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0024 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0024 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0029 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0268 | AFR | ESN | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0318 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0287 | AFR | GWD | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03579 | hp1 | a0001 | c0003 | t0003 | g0337 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0009 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03654 | hp1 | a0001 | c0003 | t0005 | g0364 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03654 | hp2 | a0001 | c0001 | t0011 | g0012 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0044 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03669 | hp2 | a0001 | c0001 | t0004 | g0156 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03688 | hp1 | a0001 | c0001 | t0004 | g0219 | SAS | STU | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0151 | SAS | STU | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03704 | hp1 | a0001 | c0001 | t0003 | g0114 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0286 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0041 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03710 | hp2 | a0001 | c0001 | t0005 | g0292 | SAS | PJL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03831 | hp1 | a0001 | c0004 | t0001 | g0358 | SAS | BEB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03831 | hp2 | a0001 | c0001 | t0004 | g0177 | SAS | BEB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0158 | SAS | BEB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03834 | hp2 | a0001 | c0001 | t0004 | g0354 | SAS | BEB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0330 | SAS | BEB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03927 | hp2 | a0001 | c0002 | t0001 | g0047 | SAS | BEB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0345 | SAS | BEB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03942 | hp2 | a0001 | c0002 | t0001 | g0078 | SAS | BEB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG04115 | hp1 | a0001 | c0001 | t0005 | g0112 | SAS | STU | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG04115 | hp2 | a0001 | c0001 | t0004 | g0327 | SAS | STU | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG04184 | hp1 | a0001 | c0001 | t0004 | g0118 | SAS | BEB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0329 | SAS | BEB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0304 | SAS | STU | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG04199 | hp2 | a0001 | c0001 | t0005 | g0113 | SAS | STU | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG04204 | hp1 | a0001 | c0001 | t0005 | g0366 | SAS | STU | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0311 | SAS | STU | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG04228 | hp1 | a0001 | c0002 | t0001 | g0235 | SAS | STU | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0042 | SAS | STU | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18522 | hp1 | a0001 | c0002 | t0001 | g0182 | AFR | YRI | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0008 | AFR | YRI | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18747 | hp2 | a0001 | c0002 | t0001 | g0004 | EAS | CHB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18906 | hp1 | a0001 | c0005 | t0001 | g0184 | AFR | YRI | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0111 | AFR | YRI | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18940 | hp1 | a0001 | c0002 | t0001 | g0376 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18941 | hp1 | a0001 | c0001 | t0005 | g0057 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18941 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0128 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18942 | hp2 | a0001 | c0001 | t0004 | g0011 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18943 | hp1 | a0001 | c0001 | t0005 | g0223 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18943 | hp2 | a0001 | c0001 | t0004 | g0099 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18944 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18946 | hp1 | a0001 | c0001 | t0005 | g0248 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18947 | hp1 | a0003 | c0006 | t0002 | g0093 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18947 | hp2 | a0001 | c0002 | t0001 | g0233 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0242 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0280 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18949 | hp2 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18951 | hp2 | a0008 | c0014 | t0001 | g0297 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18954 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18956 | hp1 | a0001 | c0001 | t0004 | g0100 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18956 | hp2 | a0001 | c0002 | t0001 | g0294 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18957 | hp1 | a0001 | c0002 | t0001 | g0017 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18957 | hp2 | a0001 | c0003 | t0002 | g0121 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18960 | hp1 | a0001 | c0002 | t0001 | g0237 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18960 | hp2 | a0001 | c0002 | t0001 | g0164 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18963 | hp1 | a0001 | c0002 | t0001 | g0225 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18963 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18964 | hp1 | a0001 | c0003 | t0004 | g0192 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18967 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18968 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0070 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0120 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18970 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18970 | hp2 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18971 | hp1 | a0001 | c0002 | t0001 | g0061 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18971 | hp2 | a0001 | c0004 | t0001 | g0205 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18972 | hp2 | a0001 | c0002 | t0001 | g0194 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18973 | hp1 | a0001 | c0002 | t0001 | g0144 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0296 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18975 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18977 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18978 | hp1 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18978 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18979 | hp1 | a0001 | c0002 | t0001 | g0069 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0013 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18980 | hp2 | a0009 | c0008 | t0009 | g0004 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0059 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18983 | hp1 | a0001 | c0002 | t0001 | g0172 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18986 | hp2 | a0001 | c0002 | t0001 | g0127 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18988 | hp1 | a0001 | c0001 | t0005 | g0229 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18988 | hp2 | a0010 | c0013 | t0001 | g0170 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18989 | hp1 | a0001 | c0001 | t0010 | g0240 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18992 | hp2 | a0001 | c0002 | t0001 | g0291 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18993 | hp1 | a0001 | c0002 | t0001 | g0218 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0143 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19000 | hp1 | a0001 | c0002 | t0001 | g0281 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0134 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19003 | hp1 | a0011 | c0009 | t0009 | g0071 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19004 | hp2 | a0001 | c0004 | t0001 | g0081 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19005 | hp1 | a0001 | c0002 | t0001 | g0142 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19005 | hp2 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19009 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0213 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19010 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19011 | hp1 | a0001 | c0004 | t0001 | g0064 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19011 | hp2 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19012 | hp1 | a0001 | c0004 | t0001 | g0117 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19012 | hp2 | a0001 | c0004 | t0001 | g0046 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0178 | AFR | LWK | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19030 | hp2 | a0001 | c0001 | t0008 | g0201 | AFR | LWK | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | LWK | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0206 | AFR | LWK | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19054 | hp1 | a0001 | c0002 | t0001 | g0004 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19056 | hp2 | a0001 | c0001 | t0004 | g0198 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0010 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19057 | hp2 | a0001 | c0004 | t0001 | g0056 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19058 | hp2 | a0001 | c0001 | t0005 | g0231 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19062 | hp2 | a0001 | c0001 | t0005 | g0226 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19063 | hp1 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19064 | hp1 | a0001 | c0001 | t0004 | g0271 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19064 | hp2 | a0003 | c0006 | t0002 | g0090 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19065 | hp1 | a0001 | c0002 | t0001 | g0254 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19066 | hp1 | a0001 | c0001 | t0005 | g0216 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0252 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19068 | hp1 | a0001 | c0002 | t0001 | g0097 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19068 | hp2 | a0001 | c0002 | t0001 | g0124 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19080 | hp2 | a0001 | c0002 | t0001 | g0298 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19081 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19082 | hp1 | a0001 | c0002 | t0001 | g0126 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19084 | hp2 | a0001 | c0004 | t0001 | g0215 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19086 | hp1 | a0001 | c0001 | t0005 | g0232 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19086 | hp2 | a0001 | c0002 | t0001 | g0195 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0060 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19087 | hp2 | a0001 | c0004 | t0001 | g0204 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19089 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19089 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19091 | hp1 | a0001 | c0001 | t0005 | g0230 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19091 | hp2 | a0001 | c0002 | t0001 | g0279 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0315 | AFR | YRI | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA19240 | hp2 | a0001 | c0001 | t0004 | g0007 | AFR | YRI | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ASW | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0149 | AFR | ASW | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA20752 | hp1 | a0001 | c0002 | t0001 | g0267 | EUR | TSI | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0361 | EUR | TSI | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA20805 | hp1 | a0001 | c0002 | t0001 | g0307 | EUR | TSI | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0023 | EUR | TSI | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0349 | SAS | GIH | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA20905 | hp2 | a0001 | c0002 | t0001 | g0309 | SAS | GIH | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0241 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0341 | AMR | CLM | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02109 | hp2 | a0001 | c0001 | t0004 | g0264 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0343 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02486 | hp2 | a0001 | c0003 | t0007 | g0260 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0299 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG02559 | hp2 | a0001 | c0003 | t0003 | g0336 | AFR | ACB | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03471 | hp1 | a0001 | c0005 | t0001 | g0276 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0344 | AFR | MSL | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG06807 | hp1 | a0001 | c0001 | t0004 | g0185 | AFR | USA | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0257 | AFR | USA | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA18955 | hp2 | a0001 | c0001 | t0005 | g0214 | EAS | JPT | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0375 | AFR | USA | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0147 | AFR | USA | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA21309 | hp1 | a0001 | c0001 | t0003 | g0207 | AFR | LWK | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | LWK | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0300 | REF | REF | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0359 | REF | REF | NUB1_chr7_151336812_151383449 | NUB1 | chr7 | 151336812 | 151383449 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:151345361 | G | T | 1 | a0002 | 2 | HG01074.hp1 HG01243.hp2 |
missense_variant | MODERATE | c.12G>T | p.Lys4Asn | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/15 | 49/3109 | 12/1848 | 4/615 | chr7 | 151345361 | |||
chr7:151345387 | A | G | 1 | a0003 | 2 | NA18947.hp1 NA19064.hp2 |
missense_variant | MODERATE | c.38A>G | p.Gln13Arg | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/15 | 75/3109 | 38/1848 | 13/615 | chr7 | 151345387 | |||
chr7:151349109 | T | G | 2 | a0009 a0011 |
2 | NA18980.hp2 NA19003.hp1 |
missense_variant | MODERATE | c.154T>G | p.Cys52Gly | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/15 | 191/3109 | 154/1848 | 52/615 | chr7 | 151349109 | |||
chr7:151355891 | A | G | 1 | a0004 | 1 | HG02027.hp2 | missense_variant | MODERATE | c.539A>G | p.Lys180Arg | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 6/15 | 576/3109 | 539/1848 | 180/615 | chr7 | 151355891 | |||
chr7:151360154 | C | T | 1 | a0011 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.707C>T | p.Ala236Val | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 744/3109 | 707/1848 | 236/615 | chr7 | 151360154 | |||
chr7:151360158 | G | A | 1 | a0011 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.711G>A | p.Met237Ile | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 748/3109 | 711/1848 | 237/615 | chr7 | 151360158 | |||
chr7:151360159 | G | T | 1 | a0011 | 1 | NA19003.hp1 | stop_gained | HIGH | c.712G>T | p.Gly238* | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 749/3109 | 712/1848 | 238/615 | chr7 | 151360159 | |||
chr7:151360160 | G | C | 1 | a0011 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.713G>C | p.Gly238Ala | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 750/3109 | 713/1848 | 238/615 | chr7 | 151360160 | |||
chr7:151360162 | T | G | 1 | a0011 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.715T>G | p.Tyr239Asp | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 752/3109 | 715/1848 | 239/615 | chr7 | 151360162 | |||
chr7:151360178 | G | T | 1 | a0011 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.731G>T | p.Arg244Ile | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 768/3109 | 731/1848 | 244/615 | chr7 | 151360178 | |||
chr7:151360184 | T | C | 1 | a0011 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.737T>C | p.Phe246Ser | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 774/3109 | 737/1848 | 246/615 | chr7 | 151360184 | |||
chr7:151360189 | A | T | 1 | a0011 | 1 | NA19003.hp1 | stop_gained | HIGH | c.742A>T | p.Lys248* | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 779/3109 | 742/1848 | 248/615 | chr7 | 151360189 | |||
chr7:151360191 | A | C | 1 | a0011 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.744A>C | p.Lys248Asn | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 781/3109 | 744/1848 | 248/615 | chr7 | 151360191 | |||
chr7:151360195 | A | C | 1 | a0011 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.748A>C | p.Lys250Gln | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 785/3109 | 748/1848 | 250/615 | chr7 | 151360195 | |||
chr7:151360200 | A | T | 1 | a0011 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.753A>T | p.Glu251Asp | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 790/3109 | 753/1848 | 251/615 | chr7 | 151360200 | |||
chr7:151360201 | T | C | 1 | a0011 | 1 | NA19003.hp1 | missense_variant | MODERATE | c.754T>C | p.Tyr252His | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 791/3109 | 754/1848 | 252/615 | chr7 | 151360201 | |||
chr7:151367016 | G | A | 1 | a0005 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.878G>A | p.Arg293His | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 9/15 | 915/3109 | 878/1848 | 293/615 | chr7 | 151367016 | |||
chr7:151367955 | A | G | 1 | a0007 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.1082A>G | p.Glu361Gly | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 10/15 | 1119/3109 | 1082/1848 | 361/615 | chr7 | 151367955 | |||
chr7:151374139 | C | T | 1 | a0006 | 1 | HG02257.hp2 | missense_variant | MODERATE | c.1291C>T | p.Arg431Cys | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/15 | 1328/3109 | 1291/1848 | 431/615 | chr7 | 151374139 | |||
chr7:151375929 | G | A | 1 | a0010 | 1 | NA18988.hp2 | missense_variant | MODERATE | c.1477G>A | p.Glu493Lys | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/15 | 1514/3109 | 1477/1848 | 493/615 | chr7 | 151375929 | |||
chr7:151376748 | G | A | 1 | a0008 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.1606G>A | p.Glu536Lys | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 14/15 | 1643/3109 | 1606/1848 | 536/615 | chr7 | 151376748 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:151355889 | C | T | 1 | a0001c0005 | 2 | HG03471.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.537C>T | p.Ala179Ala | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 6/15 | 574/3109 | 537/1848 | 179/615 | chr7 | 151355889 | |||
chr7:151360164 | T | C | 1 | a0011c0009 | 1 | NA19003.hp1 | synonymous_variant | LOW | c.717T>C | p.Tyr239Tyr | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/15 | 754/3109 | 717/1848 | 239/615 | chr7 | 151360164 | |||
chr7:151366978 | C | T | 6 | a0001c0002 a0001c0003 a0008c0014 others(3): Show |
138 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(135): Show |
synonymous_variant | LOW | c.840C>T | p.Tyr280Tyr | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 9/15 | 877/3109 | 840/1848 | 280/615 | chr7 | 151366978 | |||
chr7:151377210 | A | G | 6 | a0001c0002 a0001c0004 a0008c0014 others(3): Show |
134 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(131): Show |
synonymous_variant | LOW | c.1833A>G | p.Ala611Ala | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 1870/3109 | 1833/1848 | 611/615 | chr7 | 151377210 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:151377393 | G | A | 10 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0010 others(7): Show |
165 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*168G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 168 | chr7 | 151377393 | ||||||
chr7:151377400 | C | T | 2 | a0001c0001t0007 a0001c0003t0007 |
7 | HG02486.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*175C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 175 | chr7 | 151377400 | ||||||
chr7:151377432 | C | A | 1 | a0001c0002t0013 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*207C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 207 | chr7 | 151377432 | ||||||
chr7:151377577 | C | T | 9 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0011 others(6): Show |
164 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(161): Show |
3_prime_UTR_variant | MODIFIER | c.*352C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 352 | chr7 | 151377577 | ||||||
chr7:151377657 | G | A | 1 | a0001c0001t0011 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*432G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 432 | chr7 | 151377657 | ||||||
chr7:151377803 | G | C | 5 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0008 others(2): Show |
33 | HG00280.hp2 HG00323.hp1 HG00597.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*578G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 578 | chr7 | 151377803 | ||||||
chr7:151378071 | T | C | 1 | a0001c0001t0006 | 10 | HG02258.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*846T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 846 | chr7 | 151378071 | ||||||
chr7:151378170 | G | A | 2 | a0009c0008t0009 a0011c0009t0009 |
2 | NA18980.hp2 NA19003.hp1 |
3_prime_UTR_variant | MODIFIER | c.*945G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 945 | chr7 | 151378170 | ||||||
chr7:151378222 | A | G | 23 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0004 others(20): Show |
333 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(330): Show |
3_prime_UTR_variant | MODIFIER | c.*997A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 997 | chr7 | 151378222 | ||||||
chr7:151378237 | T | C | 5 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0012 others(2): Show |
61 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*1012T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 1012 | chr7 | 151378237 | ||||||
chr7:151378308 | G | T | 1 | a0001c0001t0012 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1083G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 15/15 | 1083 | chr7 | 151378308 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:151341872 | T | C | 273 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(270): Show |
297 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(294): Show |
intron_variant | MODIFIER | c.-3+26T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151341872 | |||||||
chr7:151341918 | C | G | 2 | a0001c0001t0002g0282 a0001c0001t0002g0283 |
2 | HG00323.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.-3+72C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151341918 | |||||||
chr7:151341931 | C | G | 1 | a0001c0002t0001g0281 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-3+85C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151341931 | |||||||
chr7:151341935 | T | C | 130 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(127): Show |
144 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.-3+89T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151341935 | |||||||
chr7:151342017 | G | A | 1 | a0001c0002t0013g0284 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-3+171G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342017 | |||||||
chr7:151342058 | T | G | 1 | a0001c0002t0001g0146 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-3+212T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342058 | |||||||
chr7:151342093 | T | C | 32 | a0001c0001t0002g0147 a0001c0001t0002g0154 a0001c0001t0002g0155 others(29): Show |
32 | HG00639.hp1 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-3+247T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342093 | |||||||
chr7:151342187 | C | G | 1 | a0001c0001t0002g0280 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-3+341C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342187 | |||||||
chr7:151342349 | A | G | 32 | a0001c0001t0002g0147 a0001c0001t0002g0154 a0001c0001t0002g0155 others(29): Show |
32 | HG00639.hp1 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-3+503A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342349 | |||||||
chr7:151342470 | G | A | 1 | a0001c0001t0004g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-3+624G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342470 | |||||||
chr7:151342638 | G | A | 1 | a0001c0001t0004g0178 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-3+792G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342638 | |||||||
chr7:151342720 | C | T | 1 | a0001c0001t0007g0145 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-3+874C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342720 | |||||||
chr7:151342757 | G | A | 1 | a0001c0001t0012g0285 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-3+911G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342757 | |||||||
chr7:151342828 | A | T | 1 | a0001c0002t0001g0279 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-3+982A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342828 | |||||||
chr7:151342864 | G | A | 1 | a0001c0002t0001g0179 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-3+1018G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342864 | |||||||
chr7:151342970 | G | A | 1 | a0001c0001t0004g0286 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-3+1124G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151342970 | |||||||
chr7:151343021 | T | C | 5 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0007g0183 others(2): Show |
5 | HG02615.hp2 HG02723.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.-3+1175T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343021 | |||||||
chr7:151343041 | A | G | 1 | a0001c0002t0001g0376 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-3+1195A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343041 | |||||||
chr7:151343092 | G | A | 5 | a0001c0001t0003g0018 a0001c0001t0003g0188 a0001c0001t0004g0185 others(2): Show |
6 | HG02572.hp1 HG02965.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-3+1246G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343092 | |||||||
chr7:151343165 | A | G | 7 | a0001c0001t0002g0275 a0001c0001t0003g0023 a0001c0001t0003g0274 others(4): Show |
8 | HG01515.hp2 HG01517.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-3+1319A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343165 | |||||||
chr7:151343246 | C | T | 2 | a0001c0001t0002g0272 a0001c0001t0004g0271 |
2 | NA19002.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-3+1400C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343246 | |||||||
chr7:151343308 | G | A | 315 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(312): Show |
349 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(346): Show |
intron_variant | MODIFIER | c.-3+1462G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343308 | |||||||
chr7:151343348 | A | G | 20 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0257 others(17): Show |
25 | HG00735.hp1 HG01255.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.-3+1502A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343348 | |||||||
chr7:151343518 | G | A | 1 | a0001c0001t0002g0287 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-3+1672G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343518 | |||||||
chr7:151343566 | T | C | 32 | a0001c0001t0002g0147 a0001c0001t0002g0154 a0001c0001t0002g0155 others(29): Show |
32 | HG00639.hp1 HG00741.hp2 HG01069.hp2 others(29): Show |
intron_variant | MODIFIER | c.-3+1720T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343566 | |||||||
chr7:151343567 | C | T | 48 | a0001c0001t0002g0021 a0001c0001t0002g0220 a0001c0001t0002g0221 others(45): Show |
50 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-3+1721C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343567 | |||||||
chr7:151343589 | G | A | 1 | a0001c0001t0006g0288 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-3+1743G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343589 | |||||||
chr7:151343600 | C | G | 49 | a0001c0001t0002g0021 a0001c0001t0002g0220 a0001c0001t0002g0221 others(46): Show |
51 | HG00423.hp2 HG00438.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-2-1748C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343600 | |||||||
chr7:151343853 | T | A | 1 | a0001c0001t0003g0329 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-2-1495T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343853 | |||||||
chr7:151343879 | A | G | 16 | a0001c0001t0003g0257 a0001c0001t0003g0259 a0001c0001t0003g0263 others(13): Show |
21 | HG00735.hp1 HG01255.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.-2-1469A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343879 | |||||||
chr7:151343985 | T | C | 1 | a0006c0011t0003g0189 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-2-1363T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151343985 | |||||||
chr7:151344033 | C | T | 1 | a0001c0003t0002g0328 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-2-1315C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344033 | |||||||
chr7:151344042 | G | T | 1 | a0001c0003t0002g0328 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-2-1306G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344042 | |||||||
chr7:151344070 | A | G | 27 | a0001c0001t0002g0140 a0001c0001t0003g0180 a0001c0001t0003g0181 others(24): Show |
32 | HG00735.hp1 HG01243.hp1 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.-2-1278A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344070 | |||||||
chr7:151344151 | A | G | 13 | a0001c0001t0003g0259 a0001c0001t0003g0263 a0001c0001t0003g0265 others(10): Show |
18 | HG00735.hp1 HG01255.hp1 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.-2-1197A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344151 | |||||||
chr7:151344167 | T | C | 2 | a0001c0002t0001g0289 a0001c0002t0001g0290 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-2-1181T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344167 | |||||||
chr7:151344176 | C | G | 1 | a0001c0001t0004g0177 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-2-1172C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344176 | |||||||
chr7:151344180 | C | CA | 33 | a0001c0001t0002g0196 a0001c0001t0003g0180 a0001c0001t0003g0206 others(30): Show |
34 | HG00099.hp1 HG00741.hp1 HG01081.hp2 others(31): Show |
intron_variant | MODIFIER | c.-2-1135dupA | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | ||||||
chr7:151344180 | C | CAA | 22 | a0001c0001t0002g0019 a0001c0001t0002g0191 a0001c0001t0002g0193 others(19): Show |
23 | HG00099.hp2 HG00280.hp1 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.-2-1136_-2-1135dup others(2): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | ||||||
chr7:151344180 | C | CAAA | 8 | a0001c0001t0004g0333 a0001c0002t0001g0291 a0001c0002t0001g0332 others(5): Show |
8 | HG00621.hp1 HG00642.hp2 HG01256.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-1137_-2-1135dup others(3): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | ||||||
chr7:151344180 | C | CAAAAAAA others(3): Show |
7 | a0001c0001t0002g0161 a0001c0001t0002g0162 a0001c0001t0003g0157 others(4): Show |
7 | HG01070.hp1 HG02148.hp2 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.-2-1144_-2-1135dup others(10): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | ||||||
chr7:151344180 | C | CAAAAAAA others(4): Show |
6 | a0001c0001t0002g0154 a0001c0001t0002g0155 a0001c0001t0003g0330 others(3): Show |
6 | HG00639.hp1 HG01192.hp1 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-1145_-2-1135dup others(11): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | ||||||
chr7:151344180 | C | CAAAAAAA others(5): Show |
4 | a0001c0001t0003g0150 a0001c0001t0003g0151 a0001c0002t0001g0148 others(1): Show |
4 | HG01346.hp2 HG02738.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-1146_-2-1135dup others(12): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | ||||||
chr7:151344180 | C | CAAAAAAA others(8): Show |
1 | a0001c0001t0002g0147 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-2-1149_-2-1135dup others(15): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | ||||||
chr7:151344180 | C | CAAAAAAA others(10): Show |
1 | a0001c0001t0004g0177 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-2-1151_-2-1135dup others(17): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | ||||||
chr7:151344180 | CA | C | 6 | a0001c0001t0003g0181 a0001c0001t0003g0212 a0001c0001t0003g0374 others(3): Show |
6 | HG01168.hp2 HG02280.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-1135delA | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | ||||||
chr7:151344180 | CAAAAAA | C | 12 | a0001c0001t0002g0167 a0001c0001t0002g0168 a0001c0001t0002g0173 others(9): Show |
12 | HG01069.hp2 HG01496.hp2 HG01943.hp1 others(9): Show |
intron_variant | MODIFIER | c.-2-1140_-2-1135del others(6): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | ||||||
chr7:151344180 | CAAAAAAA others(4): Show |
C | 15 | a0001c0001t0003g0027 a0001c0001t0003g0029 a0001c0001t0003g0317 others(12): Show |
18 | HG00597.hp2 HG01256.hp1 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.-2-1145_-2-1135del others(11): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | ||||||
chr7:151344180 | CAAAAAAA others(7): Show |
C | 5 | a0001c0001t0002g0200 a0001c0001t0003g0259 a0001c0001t0004g0006 others(2): Show |
8 | HG01255.hp1 HG01891.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-1148_-2-1135del others(14): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | ||||||
chr7:151344180 | CAAAAAAA others(8): Show |
C | 26 | a0001c0001t0002g0035 a0001c0001t0002g0038 a0001c0001t0002g0039 others(23): Show |
29 | HG00735.hp1 HG01109.hp1 HG01943.hp2 others(26): Show |
intron_variant | MODIFIER | c.-2-1149_-2-1135del others(15): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | ||||||
chr7:151344180 | CAAAAAAA others(9): Show |
C | 121 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(118): Show |
136 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.-2-1150_-2-1135del others(16): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | ||||||
chr7:151344180 | CAAAAAAA others(10): Show |
C | 3 | a0001c0001t0002g0137 a0001c0001t0002g0138 a0001c0001t0002g0139 |
3 | HG00609.hp2 HG01257.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-2-1151_-2-1135del others(17): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344180 | ||||||
chr7:151344210 | A | G | 2 | a0001c0001t0002g0272 a0001c0001t0007g0256 |
2 | HG02922.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-2-1138A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344210 | |||||||
chr7:151344211 | A | AGTAG | 14 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0003g0274 others(11): Show |
15 | HG00438.hp2 HG00673.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-2-1137_-2-1136ins others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344211 | |||||||
chr7:151344211 | A | G | 39 | a0001c0001t0002g0021 a0001c0001t0002g0245 a0001c0001t0002g0249 others(36): Show |
40 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.-2-1137A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344211 | |||||||
chr7:151344212 | A | T | 39 | a0001c0001t0002g0021 a0001c0001t0002g0245 a0001c0001t0002g0249 others(36): Show |
40 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.-2-1136A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344212 | |||||||
chr7:151344213 | A | G | 2 | a0001c0001t0002g0272 a0001c0001t0007g0256 |
2 | HG02922.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-2-1135A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344213 | |||||||
chr7:151344213 | A | T | 16 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0003g0274 others(13): Show |
17 | HG00438.hp2 HG00673.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-2-1135A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344213 | |||||||
chr7:151344214 | G | GATGT | 37 | a0001c0001t0002g0021 a0001c0001t0002g0245 a0001c0001t0002g0249 others(34): Show |
38 | HG00423.hp2 HG00609.hp1 HG00673.hp1 others(35): Show |
intron_variant | MODIFIER | c.-2-1134_-2-1133ins others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344214 | |||||||
chr7:151344214 | G | GT | 16 | a0001c0001t0002g0220 a0001c0001t0002g0221 a0001c0001t0003g0274 others(13): Show |
17 | HG00438.hp2 HG00673.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.-2-1133dupT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344214 | ||||||
chr7:151344214 | G | T | 2 | a0001c0001t0002g0272 a0001c0001t0007g0256 |
2 | HG02922.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.-2-1134G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344214 | |||||||
chr7:151344248 | T | C | 1 | a0001c0002t0001g0332 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-2-1100T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344248 | |||||||
chr7:151344300 | G | A | 1 | a0001c0001t0003g0207 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-2-1048G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344300 | |||||||
chr7:151344324 | A | G | 1 | a0001c0001t0007g0256 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-2-1024A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344324 | |||||||
chr7:151344333 | C | T | 24 | a0001c0001t0003g0018 a0001c0001t0003g0135 a0001c0001t0003g0136 others(21): Show |
30 | HG00735.hp1 HG01255.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.-2-1015C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344333 | |||||||
chr7:151344334 | G | A | 1 | a0001c0001t0002g0280 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.-2-1014G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344334 | |||||||
chr7:151344386 | C | G | 3 | a0001c0001t0002g0287 a0001c0001t0002g0315 a0001c0001t0002g0316 |
3 | HG02895.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-2-962C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344386 | |||||||
chr7:151344425 | C | T | 1 | a0001c0001t0007g0256 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-2-923C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344425 | |||||||
chr7:151344435 | C | T | 1 | a0001c0001t0003g0151 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-2-913C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344435 | |||||||
chr7:151344467 | C | T | 2 | a0001c0002t0001g0133 a0001c0002t0001g0134 |
2 | NA18970.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.-2-881C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344467 | |||||||
chr7:151344580 | G | A | 1 | a0001c0002t0001g0179 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-2-768G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344580 | |||||||
chr7:151344631 | T | A | 2 | a0001c0001t0003g0027 a0001c0001t0003g0317 |
3 | HG01256.hp1 HG01261.hp1 HG01891.hp2 |
intron_variant | MODIFIER | c.-2-717T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344631 | |||||||
chr7:151344632 | C | G | 1 | a0001c0001t0008g0203 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-2-716C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344632 | |||||||
chr7:151344683 | G | A | 4 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 others(1): Show |
4 | HG03490.hp1 HG03710.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.-2-665G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344683 | |||||||
chr7:151344739 | C | CGCCTGTA others(126): Show |
6 | a0001c0001t0002g0038 a0001c0001t0002g0129 a0001c0001t0002g0174 others(3): Show |
6 | HG01496.hp2 HG01943.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.-2-493_-2-492insTG others(131): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344739 | ||||||
chr7:151344739 | C | CGCCTGTA others(259): Show |
1 | a0001c0002t0001g0128 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-2-493_-2-492insTG others(264): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344739 | ||||||
chr7:151344739 | C | CGCCTGTA others(392): Show |
1 | a0001c0001t0002g0131 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-2-493_-2-492insTG others(397): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344739 | ||||||
chr7:151344770 | T | C | 5 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0001t0003g0270 others(2): Show |
5 | HG00735.hp2 HG01884.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-578T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344770 | |||||||
chr7:151344776 | G | A | 5 | a0001c0001t0003g0268 a0001c0001t0003g0269 a0001c0001t0003g0270 others(2): Show |
5 | HG00735.hp2 HG01884.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.-2-572G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344776 | |||||||
chr7:151344835 | A | ACTAAAAA others(146): Show |
1 | a0001c0001t0004g0130 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-2-493_-2-492insTG others(151): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr7 | 151344835 | ||||||
chr7:151344856 | C | T | 109 | a0001c0001t0002g0016 a0001c0001t0002g0021 a0001c0001t0002g0039 others(106): Show |
124 | HG00280.hp1 HG00280.hp2 HG00673.hp2 others(121): Show |
intron_variant | MODIFIER | c.-2-492C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344856 | |||||||
chr7:151344860 | C | T | 7 | a0001c0001t0003g0329 a0001c0001t0003g0353 a0001c0001t0003g0367 others(4): Show |
8 | HG00639.hp2 HG00738.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-488C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344860 | |||||||
chr7:151344861 | G | A | 1 | a0001c0002t0001g0194 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-2-487G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344861 | |||||||
chr7:151344866 | G | A | 1 | a0001c0001t0008g0203 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-2-482G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344866 | |||||||
chr7:151344868 | C | T | 258 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(255): Show |
287 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(284): Show |
intron_variant | MODIFIER | c.-2-480C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344868 | |||||||
chr7:151344869 | G | A | 6 | a0001c0001t0003g0313 a0001c0001t0003g0318 a0001c0001t0006g0008 others(3): Show |
10 | HG02258.hp2 HG02572.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-2-479G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344869 | |||||||
chr7:151344870 | C | G | 1 | a0001c0002t0001g0061 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-2-478C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344870 | |||||||
chr7:151344871 | A | G | 2 | a0001c0002t0001g0061 a0001c0002t0001g0144 |
2 | NA18971.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.-2-477A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344871 | |||||||
chr7:151344872 | T | C | 218 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0013 others(215): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.-2-476T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344872 | |||||||
chr7:151344903 | T | G | 5 | a0001c0001t0003g0027 a0001c0001t0003g0263 a0001c0001t0003g0265 others(2): Show |
6 | HG00735.hp1 HG01256.hp1 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-2-445T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344903 | |||||||
chr7:151344916 | C | G | 2 | a0001c0001t0003g0320 a0001c0005t0001g0184 |
2 | HG02630.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-2-432C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344916 | |||||||
chr7:151344917 | T | G | 7 | a0001c0001t0002g0200 a0001c0001t0003g0259 a0001c0001t0004g0022 others(4): Show |
8 | HG01891.hp1 HG02572.hp1 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.-2-431T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344917 | |||||||
chr7:151344925 | A | G | 8 | a0001c0001t0003g0041 a0001c0001t0004g0352 a0001c0002t0001g0149 others(5): Show |
8 | HG00099.hp1 HG00639.hp1 HG01074.hp1 others(5): Show |
intron_variant | MODIFIER | c.-2-423A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344925 | |||||||
chr7:151344928 | G | A | 9 | a0001c0001t0003g0041 a0001c0001t0004g0352 a0001c0001t0005g0323 others(6): Show |
9 | HG00099.hp1 HG00639.hp1 HG01074.hp1 others(6): Show |
intron_variant | MODIFIER | c.-2-420G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344928 | |||||||
chr7:151344941 | A | C | 1 | a0001c0002t0001g0017 | 2 | NA18949.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.-2-407A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344941 | |||||||
chr7:151344943 | T | C | 7 | a0001c0001t0003g0265 a0001c0001t0003g0313 a0001c0001t0006g0008 others(4): Show |
12 | HG02258.hp2 HG02451.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.-2-405T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344943 | |||||||
chr7:151344948 | C | T | 2 | a0001c0002t0001g0025 a0001c0002t0001g0302 |
3 | HG00741.hp1 HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-2-400C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344948 | |||||||
chr7:151344979 | G | A | 7 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0275 others(4): Show |
10 | HG01952.hp1 HG02145.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.-2-369G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344979 | |||||||
chr7:151344987 | G | A | 2 | a0001c0001t0002g0062 a0001c0001t0002g0280 |
2 | NA18948.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.-2-361G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344987 | |||||||
chr7:151344995 | G | A | 3 | a0001c0001t0002g0196 a0001c0001t0002g0199 a0001c0002t0001g0375 |
3 | NA18994.hp1 NA18999.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-2-353G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151344995 | |||||||
chr7:151345006 | G | A | 1 | a0001c0004t0001g0205 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-2-342G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151345006 | |||||||
chr7:151345027 | C | T | 1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-2-321C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151345027 | |||||||
chr7:151345151 | G | A | 1 | a0001c0002t0001g0063 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-2-197G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151345151 | |||||||
chr7:151345197 | A | G | 78 | a0001c0001t0002g0005 a0001c0001t0002g0013 a0001c0001t0002g0014 others(75): Show |
85 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.-2-151A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 1/14 | chr7 | 151345197 | |||||||
chr7:151345691 | C | T | 290 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(287): Show |
321 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(318): Show |
intron_variant | MODIFIER | c.117+225C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151345691 | |||||||
chr7:151346087 | T | A | 1 | a0001c0001t0002g0039 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.117+621T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346087 | |||||||
chr7:151346135 | T | C | 18 | a0001c0001t0002g0043 a0001c0001t0002g0147 a0001c0001t0002g0154 others(15): Show |
23 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.117+669T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346135 | |||||||
chr7:151346186 | G | T | 46 | a0001c0001t0002g0140 a0001c0001t0002g0200 a0001c0001t0003g0018 others(43): Show |
55 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(52): Show |
intron_variant | MODIFIER | c.117+720G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346186 | |||||||
chr7:151346195 | T | G | 1 | a0001c0001t0003g0158 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.117+729T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346195 | |||||||
chr7:151346199 | T | A | 1 | a0001c0001t0003g0158 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.117+733T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346199 | |||||||
chr7:151346200 | T | A | 1 | a0001c0001t0003g0158 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.117+734T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346200 | |||||||
chr7:151346242 | C | T | 1 | a0001c0001t0004g0352 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.117+776C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346242 | |||||||
chr7:151346427 | G | C | 1 | a0001c0001t0002g0038 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.117+961G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346427 | |||||||
chr7:151346584 | G | T | 48 | a0001c0001t0002g0039 a0001c0001t0002g0140 a0001c0001t0002g0200 others(45): Show |
57 | HG00423.hp1 HG01069.hp1 HG01071.hp2 others(54): Show |
intron_variant | MODIFIER | c.117+1118G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346584 | |||||||
chr7:151346614 | G | A | 309 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(306): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(338): Show |
intron_variant | MODIFIER | c.117+1148G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346614 | |||||||
chr7:151346643 | G | T | 3 | a0001c0001t0002g0287 a0001c0001t0002g0315 a0001c0001t0002g0316 |
3 | HG02895.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.117+1177G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346643 | |||||||
chr7:151346661 | C | T | 8 | a0001c0001t0002g0043 a0001c0001t0002g0147 a0001c0001t0002g0154 others(5): Show |
8 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+1195C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346661 | |||||||
chr7:151346726 | C | G | 1 | a0001c0004t0001g0204 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.117+1260C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346726 | |||||||
chr7:151346770 | G | T | 5 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0268 others(2): Show |
5 | HG00735.hp2 HG01884.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+1304G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346770 | |||||||
chr7:151346901 | G | A | 5 | a0001c0001t0007g0107 a0001c0001t0007g0132 a0001c0001t0007g0145 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+1435G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346901 | |||||||
chr7:151346949 | G | A | 314 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(311): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.117+1483G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151346949 | |||||||
chr7:151347271 | G | A | 1 | a0001c0001t0004g0079 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.118-1802G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347271 | |||||||
chr7:151347326 | C | T | 5 | a0001c0001t0007g0107 a0001c0001t0007g0132 a0001c0001t0007g0145 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-1747C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347326 | |||||||
chr7:151347418 | G | GA | 314 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(311): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.118-1646dupA | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151347418 | ||||||
chr7:151347450 | T | C | 1 | a0001c0001t0003g0348 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.118-1623T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347450 | |||||||
chr7:151347464 | T | C | 1 | a0001c0001t0004g0130 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.118-1609T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347464 | |||||||
chr7:151347466 | C | T | 1 | a0001c0001t0004g0130 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.118-1607C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347466 | |||||||
chr7:151347490 | A | C | 22 | a0001c0001t0004g0007 a0001c0001t0004g0024 a0001c0001t0004g0032 others(19): Show |
26 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.118-1583A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347490 | |||||||
chr7:151347503 | G | T | 5 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0268 others(2): Show |
5 | HG00735.hp2 HG01884.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-1570G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347503 | |||||||
chr7:151347505 | T | C | 287 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(284): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(309): Show |
intron_variant | MODIFIER | c.118-1568T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347505 | |||||||
chr7:151347571 | C | T | 25 | a0001c0001t0002g0140 a0001c0001t0002g0200 a0001c0001t0003g0018 others(22): Show |
30 | HG00423.hp1 HG01243.hp1 HG01884.hp1 others(27): Show |
intron_variant | MODIFIER | c.118-1502C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347571 | |||||||
chr7:151347671 | G | A | 5 | a0001c0001t0007g0107 a0001c0001t0007g0132 a0001c0001t0007g0145 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-1402G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347671 | |||||||
chr7:151347749 | G | A | 5 | a0001c0001t0004g0032 a0001c0001t0004g0156 a0001c0001t0004g0219 others(2): Show |
6 | HG01069.hp1 HG01071.hp2 HG01106.hp1 others(3): Show |
intron_variant | MODIFIER | c.118-1324G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347749 | |||||||
chr7:151347752 | C | A | 18 | a0001c0001t0002g0043 a0001c0001t0002g0147 a0001c0001t0002g0154 others(15): Show |
23 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.118-1321C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347752 | |||||||
chr7:151347807 | C | G | 3 | a0001c0002t0001g0063 a0001c0002t0001g0104 a0001c0003t0002g0105 |
3 | HG00408.hp1 HG02080.hp1 HG02155.hp2 |
intron_variant | MODIFIER | c.118-1266C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347807 | |||||||
chr7:151347847 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.118-1226G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347847 | |||||||
chr7:151347943 | A | T | 18 | a0001c0001t0002g0043 a0001c0001t0002g0147 a0001c0001t0002g0154 others(15): Show |
23 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.118-1130A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347943 | |||||||
chr7:151347978 | C | T | 1 | a0001c0002t0001g0310 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.118-1095C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151347978 | |||||||
chr7:151348075 | A | G | 2 | a0001c0001t0002g0140 a0001c0001t0002g0200 |
2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.118-998A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348075 | |||||||
chr7:151348237 | A | G | 2 | a0001c0002t0001g0325 a0001c0003t0002g0306 |
2 | HG00140.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.118-836A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348237 | |||||||
chr7:151348353 | A | T | 1 | a0001c0002t0001g0106 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.118-720A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348353 | |||||||
chr7:151348370 | G | C | 1 | a0001c0001t0004g0271 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.118-703G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348370 | |||||||
chr7:151348479 | T | C | 336 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(333): Show |
373 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(370): Show |
intron_variant | MODIFIER | c.118-594T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348479 | |||||||
chr7:151348569 | C | CT | 9 | a0001c0001t0002g0140 a0001c0001t0002g0200 a0001c0001t0003g0042 others(6): Show |
9 | HG00438.hp2 HG00735.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.118-480dupT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151348569 | ||||||
chr7:151348569 | C | CTT | 23 | a0001c0001t0004g0067 a0001c0001t0004g0159 a0001c0001t0004g0286 others(20): Show |
24 | HG00099.hp1 HG01517.hp1 HG03041.hp1 others(21): Show |
intron_variant | MODIFIER | c.118-481_118-480dup others(2): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151348569 | ||||||
chr7:151348569 | C | CTTT | 120 | a0001c0001t0002g0001 a0001c0001t0002g0196 a0001c0001t0002g0199 others(117): Show |
129 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.118-482_118-480dup others(3): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151348569 | ||||||
chr7:151348569 | C | CTTTT | 39 | a0001c0001t0001g0365 a0001c0001t0003g0314 a0001c0001t0003g0330 others(36): Show |
39 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.118-483_118-480dup others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151348569 | ||||||
chr7:151348569 | CTT | C | 8 | a0001c0001t0002g0168 a0001c0001t0003g0313 a0001c0001t0006g0008 others(5): Show |
13 | HG01993.hp1 HG02258.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.118-481_118-480del others(2): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151348569 | ||||||
chr7:151348569 | CTTT | C | 7 | a0001c0001t0002g0043 a0001c0001t0002g0147 a0001c0001t0002g0154 others(4): Show |
7 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-482_118-480del others(3): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151348569 | ||||||
chr7:151348569 | CTTTT | C | 13 | a0001c0001t0002g0058 a0001c0001t0002g0091 a0001c0001t0002g0092 others(10): Show |
14 | HG00099.hp2 HG00597.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.118-483_118-480del others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151348569 | ||||||
chr7:151348569 | CTTTTT | C | 87 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(84): Show |
104 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.118-484_118-480del others(5): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151348569 | ||||||
chr7:151348569 | CTTTTTT | C | 25 | a0001c0001t0003g0034 a0001c0001t0003g0277 a0001c0001t0003g0326 others(22): Show |
29 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.118-485_118-480del others(6): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151348569 | ||||||
chr7:151348569 | CTTTTTTT others(3): Show |
C | 1 | a0001c0003t0007g0260 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.118-489_118-480del others(10): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr7 | 151348569 | ||||||
chr7:151348710 | G | A | 3 | a0001c0001t0002g0287 a0001c0001t0002g0315 a0001c0001t0002g0316 |
3 | HG02895.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.118-363G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348710 | |||||||
chr7:151348818 | G | A | 5 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0268 others(2): Show |
5 | HG00735.hp2 HG01884.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-255G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348818 | |||||||
chr7:151348903 | C | G | 335 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(332): Show |
372 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(369): Show |
intron_variant | MODIFIER | c.118-170C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348903 | |||||||
chr7:151348908 | C | G | 5 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0268 others(2): Show |
5 | HG00735.hp2 HG01884.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-165C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348908 | |||||||
chr7:151348936 | A | G | 313 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(310): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(343): Show |
intron_variant | MODIFIER | c.118-137A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348936 | |||||||
chr7:151348961 | G | A | 1 | a0001c0002t0001g0068 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.118-112G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151348961 | |||||||
chr7:151349020 | T | A | 1 | a0001c0001t0004g0130 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.118-53T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151349020 | |||||||
chr7:151349032 | T | A | 1 | a0001c0001t0004g0156 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.118-41T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 2/14 | chr7 | 151349032 | |||||||
chr7:151349534 | C | G | 1 | a0001c0001t0004g0271 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.285+294C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151349534 | |||||||
chr7:151349563 | C | T | 174 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(171): Show |
191 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.285+323C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151349563 | |||||||
chr7:151349643 | A | G | 5 | a0001c0001t0007g0107 a0001c0001t0007g0132 a0001c0001t0007g0145 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.285+403A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151349643 | |||||||
chr7:151349663 | C | T | 1 | a0001c0002t0001g0322 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.285+423C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151349663 | |||||||
chr7:151349746 | A | G | 314 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(311): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(344): Show |
intron_variant | MODIFIER | c.285+506A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151349746 | |||||||
chr7:151349810 | C | T | 96 | a0001c0001t0002g0196 a0001c0001t0002g0199 a0001c0001t0003g0158 others(93): Show |
101 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.285+570C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151349810 | |||||||
chr7:151349915 | C | G | 258 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(255): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.285+675C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151349915 | |||||||
chr7:151350035 | C | T | 2 | a0003c0006t0002g0090 a0003c0006t0002g0093 |
2 | NA18947.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.285+795C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350035 | |||||||
chr7:151350056 | G | A | 230 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(227): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(249): Show |
intron_variant | MODIFIER | c.285+816G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350056 | |||||||
chr7:151350060 | G | C | 3 | a0001c0001t0002g0287 a0001c0001t0002g0315 a0001c0001t0002g0316 |
3 | HG02895.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.285+820G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350060 | |||||||
chr7:151350291 | C | A | 11 | a0001c0002t0001g0010 a0001c0002t0001g0069 a0001c0002t0001g0094 others(8): Show |
12 | NA18947.hp2 NA18951.hp2 NA18956.hp2 others(9): Show |
intron_variant | MODIFIER | c.285+1051C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350291 | |||||||
chr7:151350412 | T | G | 24 | a0001c0001t0002g0249 a0001c0001t0003g0206 a0001c0001t0003g0348 others(21): Show |
25 | HG00280.hp2 HG00597.hp2 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.286-1012T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350412 | |||||||
chr7:151350424 | A | G | 339 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(336): Show |
376 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(373): Show |
intron_variant | MODIFIER | c.286-1000A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350424 | |||||||
chr7:151350459 | A | G | 25 | a0001c0001t0002g0249 a0001c0001t0003g0206 a0001c0001t0003g0274 others(22): Show |
26 | HG00280.hp2 HG00597.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.286-965A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350459 | |||||||
chr7:151350519 | A | G | 1 | a0001c0001t0002g0140 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.286-905A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350519 | |||||||
chr7:151350558 | C | T | 1 | a0001c0001t0002g0139 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.286-866C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350558 | |||||||
chr7:151350562 | G | C | 2 | a0001c0001t0002g0013 a0001c0001t0002g0080 |
3 | HG00438.hp1 NA18944.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.286-862G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350562 | |||||||
chr7:151350585 | G | C | 181 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(178): Show |
198 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.286-839G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350585 | |||||||
chr7:151350692 | C | T | 1 | a0001c0002t0001g0254 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.286-732C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350692 | |||||||
chr7:151350764 | C | T | 1 | a0001c0002t0001g0061 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.286-660C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350764 | |||||||
chr7:151350861 | A | G | 258 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(255): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.286-563A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350861 | |||||||
chr7:151350897 | C | CCA | 7 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0045 others(4): Show |
9 | HG00438.hp1 HG00621.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.286-527_286-526ins others(2): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350897 | |||||||
chr7:151350898 | G | C | 7 | a0001c0001t0002g0013 a0001c0001t0002g0014 a0001c0001t0002g0045 others(4): Show |
9 | HG00438.hp1 HG00621.hp2 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.286-526G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350898 | |||||||
chr7:151350900 | T | C | 1 | a0001c0005t0001g0184 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.286-524T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350900 | |||||||
chr7:151350926 | A | G | 256 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(253): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.286-498A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350926 | |||||||
chr7:151350941 | G | A | 1 | a0001c0002t0001g0228 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.286-483G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151350941 | |||||||
chr7:151351398 | G | A | 270 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(267): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(290): Show |
intron_variant | MODIFIER | c.286-26G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 3/14 | chr7 | 151351398 | |||||||
chr7:151351621 | G | A | 1 | a0001c0001t0007g0186 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.344+139G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151351621 | |||||||
chr7:151351830 | T | C | 6 | a0001c0001t0002g0039 a0001c0001t0007g0107 a0001c0001t0007g0132 others(3): Show |
6 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.344+348T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151351830 | |||||||
chr7:151351863 | A | G | 5 | a0001c0001t0004g0007 a0001c0001t0004g0111 a0001c0001t0004g0185 others(2): Show |
7 | HG02109.hp2 HG02145.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.344+381A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151351863 | |||||||
chr7:151351873 | G | A | 1 | a0001c0002t0001g0261 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.344+391G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151351873 | |||||||
chr7:151351916 | A | AAC | 45 | a0001c0001t0003g0023 a0001c0001t0003g0027 a0001c0001t0003g0029 others(42): Show |
48 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(45): Show |
intron_variant | MODIFIER | c.344+453_344+454dup others(2): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 151351916 | ||||||
chr7:151351916 | A | AACAC | 33 | a0001c0001t0002g0140 a0001c0001t0002g0200 a0001c0001t0003g0034 others(30): Show |
37 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.344+451_344+454dup others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 151351916 | ||||||
chr7:151351916 | A | AACACAC | 36 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0275 others(33): Show |
40 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(37): Show |
intron_variant | MODIFIER | c.344+449_344+454dup others(6): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 151351916 | ||||||
chr7:151351916 | A | AACACACA others(1): Show |
53 | a0001c0001t0002g0249 a0001c0001t0003g0018 a0001c0001t0003g0188 others(50): Show |
60 | HG00280.hp2 HG00423.hp1 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.344+447_344+454dup others(8): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 151351916 | ||||||
chr7:151351916 | A | AACACACA others(3): Show |
8 | a0001c0001t0002g0039 a0001c0001t0003g0313 a0001c0001t0005g0112 others(5): Show |
13 | HG02258.hp2 HG02572.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.344+445_344+454dup others(10): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 151351916 | ||||||
chr7:151351916 | A | AACACACA others(5): Show |
11 | a0001c0001t0002g0043 a0001c0001t0002g0147 a0001c0001t0002g0154 others(8): Show |
11 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(8): Show |
intron_variant | MODIFIER | c.344+443_344+454dup others(12): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 151351916 | ||||||
chr7:151351916 | A | AACACACA others(7): Show |
8 | a0001c0001t0007g0107 a0001c0001t0007g0132 a0001c0001t0007g0145 others(5): Show |
8 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.344+441_344+454dup others(14): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 151351916 | ||||||
chr7:151351916 | A | AACACACA others(9): Show |
1 | a0001c0001t0003g0202 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.344+439_344+454dup others(16): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr7 | 151351916 | ||||||
chr7:151351916 | A | ATCACACA others(1): Show |
95 | a0001c0001t0002g0196 a0001c0001t0002g0199 a0001c0001t0003g0033 others(92): Show |
100 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.344+434_344+435ins others(8): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151351916 | |||||||
chr7:151351916 | A | ATCACACA others(3): Show |
77 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(74): Show |
89 | HG00408.hp2 HG00438.hp1 HG00597.hp1 others(86): Show |
intron_variant | MODIFIER | c.344+434_344+435ins others(10): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151351916 | |||||||
chr7:151351916 | A | ATCACACA others(5): Show |
5 | a0001c0001t0002g0051 a0001c0001t0002g0083 a0001c0001t0002g0155 others(2): Show |
5 | HG00323.hp2 HG00609.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.344+434_344+435ins others(12): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151351916 | |||||||
chr7:151351916 | A | ATCACACA others(7): Show |
1 | a0001c0001t0002g0050 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.344+434_344+435ins others(14): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151351916 | |||||||
chr7:151351917 | A | T | 1 | a0001c0003t0002g0105 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.344+435A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151351917 | |||||||
chr7:151351939 | T | C | 305 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(302): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(335): Show |
intron_variant | MODIFIER | c.344+457T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151351939 | |||||||
chr7:151352145 | C | T | 282 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(279): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.344+663C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352145 | |||||||
chr7:151352251 | A | G | 337 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(334): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(371): Show |
intron_variant | MODIFIER | c.345-561A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352251 | |||||||
chr7:151352293 | G | A | 5 | a0001c0001t0002g0140 a0001c0001t0002g0200 a0001c0001t0003g0034 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.345-519G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352293 | |||||||
chr7:151352321 | A | G | 2 | a0001c0001t0002g0140 a0001c0001t0002g0200 |
2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.345-491A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352321 | |||||||
chr7:151352417 | A | C | 183 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(180): Show |
200 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(197): Show |
intron_variant | MODIFIER | c.345-395A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352417 | |||||||
chr7:151352443 | A | T | 11 | a0001c0001t0004g0028 a0001c0001t0004g0067 a0001c0001t0004g0159 others(8): Show |
12 | HG00099.hp1 HG02647.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-369A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352443 | |||||||
chr7:151352512 | T | C | 6 | a0001c0001t0003g0313 a0001c0001t0006g0008 a0001c0001t0006g0009 others(3): Show |
11 | HG02258.hp2 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.345-300T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352512 | |||||||
chr7:151352537 | G | A | 11 | a0001c0001t0004g0028 a0001c0001t0004g0067 a0001c0001t0004g0159 others(8): Show |
12 | HG00099.hp1 HG02647.hp1 HG02896.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-275G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352537 | |||||||
chr7:151352620 | T | A | 1 | a0001c0001t0002g0091 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.345-192T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352620 | |||||||
chr7:151352621 | T | G | 1 | a0001c0001t0007g0186 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.345-191T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352621 | |||||||
chr7:151352630 | A | C | 12 | a0001c0001t0002g0039 a0001c0001t0003g0313 a0001c0001t0006g0008 others(9): Show |
17 | HG02258.hp2 HG02572.hp1 HG02572.hp2 others(14): Show |
intron_variant | MODIFIER | c.345-182A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352630 | |||||||
chr7:151352653 | G | T | 1 | a0001c0001t0003g0042 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.345-159G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352653 | |||||||
chr7:151352720 | G | A | 2 | a0001c0003t0002g0036 a0001c0003t0003g0337 |
2 | HG01109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.345-92G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352720 | |||||||
chr7:151352732 | C | G | 12 | a0001c0001t0002g0043 a0001c0001t0002g0147 a0001c0001t0002g0154 others(9): Show |
12 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.345-80C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352732 | |||||||
chr7:151352732 | C | T | 258 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(255): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.345-80C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352732 | |||||||
chr7:151352736 | C | T | 2 | a0001c0001t0003g0311 a0001c0001t0003g0355 |
2 | HG02683.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.345-76C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 4/14 | chr7 | 151352736 | |||||||
chr7:151352897 | G | A | 12 | a0001c0001t0002g0043 a0001c0001t0002g0147 a0001c0001t0002g0154 others(9): Show |
12 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.415+15G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151352897 | |||||||
chr7:151352942 | C | A | 1 | a0001c0001t0003g0265 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.415+60C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151352942 | |||||||
chr7:151353012 | G | A | 1 | a0001c0001t0005g0363 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.415+130G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353012 | |||||||
chr7:151353072 | T | C | 282 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(279): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.415+190T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353072 | |||||||
chr7:151353147 | A | C | 23 | a0001c0001t0002g0249 a0001c0001t0003g0206 a0001c0001t0003g0274 others(20): Show |
24 | HG00280.hp2 HG00597.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.415+265A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353147 | |||||||
chr7:151353187 | A | G | 1 | a0001c0002t0001g0110 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.415+305A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353187 | |||||||
chr7:151353197 | G | C | 5 | a0001c0001t0007g0107 a0001c0001t0007g0132 a0001c0001t0007g0145 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.415+315G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353197 | |||||||
chr7:151353318 | A | G | 337 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(334): Show |
374 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(371): Show |
intron_variant | MODIFIER | c.415+436A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353318 | |||||||
chr7:151353528 | C | T | 74 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(71): Show |
86 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.415+646C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353528 | |||||||
chr7:151353535 | A | G | 2 | a0001c0001t0002g0140 a0001c0001t0002g0200 |
2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.415+653A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353535 | |||||||
chr7:151353633 | C | T | 1 | a0001c0001t0002g0066 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.415+751C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353633 | |||||||
chr7:151353666 | A | G | 6 | a0001c0001t0002g0039 a0001c0001t0007g0107 a0001c0001t0007g0132 others(3): Show |
6 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.415+784A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353666 | |||||||
chr7:151353722 | C | A | 38 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0275 others(35): Show |
42 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.415+840C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353722 | |||||||
chr7:151353733 | T | C | 1 | a0001c0001t0007g0256 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.415+851T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353733 | |||||||
chr7:151353734 | G | A | 1 | a0001c0001t0003g0259 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.415+852G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353734 | |||||||
chr7:151353750 | G | A | 1 | a0001c0001t0003g0345 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.415+868G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151353750 | |||||||
chr7:151354215 | G | T | 1 | a0001c0001t0005g0057 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.415+1333G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151354215 | |||||||
chr7:151354322 | C | CT | 12 | a0001c0001t0002g0043 a0001c0001t0002g0147 a0001c0001t0002g0154 others(9): Show |
12 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.416-1431dupT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr7 | 151354322 | ||||||
chr7:151354322 | CT | C | 6 | a0001c0001t0002g0019 a0001c0001t0002g0174 a0001c0001t0003g0278 others(3): Show |
7 | HG01515.hp2 HG01943.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.416-1431delT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr7 | 151354322 | ||||||
chr7:151354397 | G | A | 5 | a0001c0001t0004g0007 a0001c0001t0004g0111 a0001c0001t0004g0185 others(2): Show |
7 | HG02109.hp2 HG02145.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.416-1371G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151354397 | |||||||
chr7:151354418 | A | T | 1 | a0001c0002t0001g0110 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.416-1350A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151354418 | |||||||
chr7:151354437 | G | A | 1 | a0001c0001t0004g0360 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.416-1331G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151354437 | |||||||
chr7:151354524 | T | C | 14 | a0001c0001t0004g0011 a0001c0001t0004g0012 a0001c0001t0004g0049 others(11): Show |
15 | HG00423.hp1 HG02015.hp2 HG02056.hp1 others(12): Show |
intron_variant | MODIFIER | c.416-1244T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151354524 | |||||||
chr7:151354715 | A | T | 1 | a0001c0001t0005g0057 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.416-1053A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151354715 | |||||||
chr7:151354719 | C | T | 8 | a0001c0001t0002g0043 a0001c0001t0002g0147 a0001c0001t0002g0154 others(5): Show |
8 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.416-1049C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151354719 | |||||||
chr7:151355043 | TG | T | 23 | a0001c0001t0002g0249 a0001c0001t0003g0206 a0001c0001t0003g0274 others(20): Show |
24 | HG00280.hp2 HG00597.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.416-723delG | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr7 | 151355043 | ||||||
chr7:151355061 | G | A | 276 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(273): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(296): Show |
intron_variant | MODIFIER | c.416-707G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151355061 | |||||||
chr7:151355211 | C | T | 282 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(279): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.416-557C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151355211 | |||||||
chr7:151355261 | T | A | 1 | a0001c0001t0007g0256 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.416-507T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151355261 | |||||||
chr7:151355281 | G | A | 2 | a0001c0005t0001g0184 a0001c0005t0001g0276 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.416-487G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151355281 | |||||||
chr7:151355613 | T | C | 282 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(279): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(307): Show |
intron_variant | MODIFIER | c.416-155T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151355613 | |||||||
chr7:151355633 | A | C | 6 | a0001c0001t0003g0313 a0001c0001t0006g0008 a0001c0001t0006g0009 others(3): Show |
11 | HG02258.hp2 HG02572.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.416-135A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151355633 | |||||||
chr7:151355760 | T | A | 3 | a0001c0002t0001g0235 a0001c0002t0001g0241 a0001c0002t0001g0340 |
3 | HG01123.hp1 HG01517.hp1 HG04228.hp1 |
splice_region_variant&intron_variant | LOW | c.416-8T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 5/14 | chr7 | 151355760 | |||||||
chr7:151355957 | A | G | 270 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(267): Show |
298 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(295): Show |
splice_region_variant&intron_variant | LOW | c.598+7A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 6/14 | chr7 | 151355957 | |||||||
chr7:151356002 | G | A | 1 | a0001c0001t0004g0324 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.598+52G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 6/14 | chr7 | 151356002 | |||||||
chr7:151356075 | C | T | 2 | a0001c0002t0001g0074 a0001c0002t0001g0146 |
2 | HG02027.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.599-53C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 6/14 | chr7 | 151356075 | |||||||
chr7:151356118 | T | C | 8 | a0001c0001t0002g0043 a0001c0001t0002g0147 a0001c0001t0002g0154 others(5): Show |
8 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.599-10T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 6/14 | chr7 | 151356118 | |||||||
chr7:151356358 | T | C | 1 | a0001c0001t0002g0115 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.693+136T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151356358 | |||||||
chr7:151356458 | T | G | 8 | a0001c0001t0002g0043 a0001c0001t0002g0147 a0001c0001t0002g0154 others(5): Show |
8 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.693+236T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151356458 | |||||||
chr7:151356474 | A | C | 1 | a0010c0013t0001g0170 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.693+252A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151356474 | |||||||
chr7:151356547 | C | A | 38 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0275 others(35): Show |
42 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.693+325C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151356547 | |||||||
chr7:151356721 | G | T | 5 | a0001c0001t0004g0007 a0001c0001t0004g0111 a0001c0001t0004g0185 others(2): Show |
7 | HG02109.hp2 HG02145.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.693+499G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151356721 | |||||||
chr7:151356721 | GT | G | 281 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(278): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.693+506delT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151356721 | ||||||
chr7:151356925 | C | T | 2 | a0001c0002t0001g0233 a0001c0002t0001g0298 |
2 | NA18947.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.693+703C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151356925 | |||||||
chr7:151356944 | C | T | 1 | a0001c0001t0003g0346 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.693+722C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151356944 | |||||||
chr7:151356978 | A | G | 1 | a0001c0001t0002g0103 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.693+756A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151356978 | |||||||
chr7:151357006 | C | T | 2 | a0001c0003t0002g0334 a0001c0003t0002g0335 |
2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.693+784C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151357006 | |||||||
chr7:151357083 | C | T | 21 | a0001c0001t0002g0249 a0001c0001t0003g0206 a0001c0001t0003g0274 others(18): Show |
22 | HG00280.hp2 HG00597.hp2 HG01361.hp1 others(19): Show |
intron_variant | MODIFIER | c.693+861C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151357083 | |||||||
chr7:151357087 | G | A | 1 | a0001c0001t0004g0211 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.693+865G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151357087 | |||||||
chr7:151357127 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.693+905C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151357127 | |||||||
chr7:151357128 | C | T | 2 | a0001c0002t0001g0142 a0001c0002t0001g0143 |
2 | NA18994.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.693+906C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151357128 | |||||||
chr7:151357183 | ATTT | A | 266 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(263): Show |
294 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.693+979_693+981del others(3): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151357183 | ||||||
chr7:151357183 | ATTTT | A | 8 | a0001c0001t0002g0191 a0001c0001t0002g0316 a0001c0001t0004g0286 others(5): Show |
8 | HG01192.hp2 HG02895.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.693+978_693+981del others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151357183 | ||||||
chr7:151357270 | C | T | 6 | a0001c0001t0002g0039 a0001c0001t0007g0107 a0001c0001t0007g0132 others(3): Show |
6 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.693+1048C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151357270 | |||||||
chr7:151357502 | T | C | 3 | a0001c0001t0003g0034 a0001c0001t0003g0277 a0001c0001t0003g0326 |
3 | HG02280.hp2 HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.693+1280T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151357502 | |||||||
chr7:151357506 | G | A | 1 | a0001c0002t0001g0222 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.693+1284G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151357506 | |||||||
chr7:151357608 | G | GT | 7 | a0001c0001t0002g0080 a0001c0001t0002g0082 a0001c0001t0002g0096 others(4): Show |
7 | HG00438.hp1 HG02080.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.693+1402dupT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151357608 | ||||||
chr7:151357608 | GT | G | 114 | a0001c0001t0002g0039 a0001c0001t0002g0043 a0001c0001t0002g0147 others(111): Show |
130 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.693+1402delT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151357608 | ||||||
chr7:151357672 | C | T | 76 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(73): Show |
88 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.693+1450C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151357672 | |||||||
chr7:151357910 | G | A | 22 | a0001c0001t0004g0007 a0001c0001t0004g0024 a0001c0001t0004g0032 others(19): Show |
26 | HG01069.hp1 HG01071.hp2 HG01074.hp1 others(23): Show |
intron_variant | MODIFIER | c.693+1688G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151357910 | |||||||
chr7:151358013 | G | A | 180 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(177): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(201): Show |
intron_variant | MODIFIER | c.693+1791G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151358013 | |||||||
chr7:151358164 | G | A | 3 | a0001c0001t0002g0287 a0001c0001t0002g0315 a0001c0001t0002g0316 |
3 | HG02895.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.693+1942G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151358164 | |||||||
chr7:151358329 | C | T | 2 | a0001c0001t0002g0055 a0001c0001t0002g0137 |
2 | HG01257.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.694-1812C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151358329 | |||||||
chr7:151358391 | G | T | 1 | a0005c0010t0003g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.694-1750G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151358391 | |||||||
chr7:151358443 | AG | A | 5 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0026 others(2): Show |
10 | HG02258.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.694-1696delG | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151358443 | ||||||
chr7:151358461 | G | A | 2 | a0001c0001t0003g0018 a0001c0001t0003g0188 |
3 | HG02970.hp2 HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.694-1680G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151358461 | |||||||
chr7:151358472 | A | G | 320 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(317): Show |
357 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(354): Show |
intron_variant | MODIFIER | c.694-1669A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151358472 | |||||||
chr7:151358860 | C | T | 2 | a0001c0005t0001g0184 a0001c0005t0001g0276 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.694-1281C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151358860 | |||||||
chr7:151358926 | G | A | 1 | a0001c0001t0002g0038 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.694-1215G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151358926 | |||||||
chr7:151359105 | A | G | 25 | a0001c0001t0002g0249 a0001c0001t0003g0206 a0001c0001t0003g0274 others(22): Show |
26 | HG00280.hp2 HG00597.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.694-1036A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359105 | |||||||
chr7:151359132 | CTAGATGA others(6): Show |
C | 1 | a0011c0009t0009g0071 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.694-1008_694-996de others(14): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359132 | |||||||
chr7:151359136 | A | G | 4 | a0001c0001t0004g0011 a0001c0001t0004g0049 a0001c0001t0004g0099 others(1): Show |
5 | HG02132.hp2 NA18941.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.694-1005A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359136 | |||||||
chr7:151359161 | G | A | 2 | a0001c0005t0001g0184 a0001c0005t0001g0276 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.694-980G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359161 | |||||||
chr7:151359166 | C | T | 1 | a0011c0009t0009g0071 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.694-975C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359166 | |||||||
chr7:151359265 | T | C | 1 | a0001c0001t0002g0085 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.694-876T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359265 | |||||||
chr7:151359282 | C | CA | 45 | a0001c0001t0003g0018 a0001c0001t0003g0034 a0001c0001t0003g0180 others(42): Show |
53 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(50): Show |
intron_variant | MODIFIER | c.694-848dupA | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151359282 | ||||||
chr7:151359282 | C | CAA | 8 | a0001c0001t0002g0140 a0001c0001t0002g0200 a0001c0001t0004g0024 others(5): Show |
9 | HG01074.hp1 HG01243.hp1 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.694-849_694-848dup others(2): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151359282 | ||||||
chr7:151359367 | T | C | 77 | a0001c0001t0002g0043 a0001c0001t0002g0140 a0001c0001t0002g0147 others(74): Show |
91 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(88): Show |
intron_variant | MODIFIER | c.694-774T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359367 | |||||||
chr7:151359384 | A | G | 5 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0026 others(2): Show |
10 | HG02258.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.694-757A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359384 | |||||||
chr7:151359442 | C | CA | 53 | a0001c0001t0003g0018 a0001c0001t0003g0034 a0001c0001t0003g0180 others(50): Show |
62 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.694-686dupA | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151359442 | ||||||
chr7:151359507 | C | CGTGGCTC others(36): Show |
5 | a0001c0001t0007g0107 a0001c0001t0007g0132 a0001c0001t0007g0145 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.694-632_694-590dup others(43): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151359507 | ||||||
chr7:151359516 | C | T | 1 | a0001c0001t0002g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.694-625C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359516 | |||||||
chr7:151359517 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.694-624G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359517 | |||||||
chr7:151359527 | C | T | 5 | a0001c0001t0003g0329 a0001c0001t0003g0350 a0001c0001t0003g0353 others(2): Show |
5 | HG00738.hp2 HG01081.hp2 HG01168.hp2 others(2): Show |
intron_variant | MODIFIER | c.694-614C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359527 | |||||||
chr7:151359670 | G | A | 25 | a0001c0001t0002g0249 a0001c0001t0003g0206 a0001c0001t0003g0274 others(22): Show |
26 | HG00280.hp2 HG00597.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.694-471G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359670 | |||||||
chr7:151359725 | C | T | 27 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0268 others(24): Show |
31 | HG00735.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.694-416C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359725 | |||||||
chr7:151359772 | G | A | 51 | a0001c0001t0002g0140 a0001c0001t0002g0200 a0001c0001t0003g0018 others(48): Show |
60 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.694-369G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359772 | |||||||
chr7:151359776 | C | CA | 21 | a0001c0001t0003g0018 a0001c0001t0003g0188 a0001c0001t0003g0210 others(18): Show |
26 | HG00423.hp1 HG01884.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.694-358dupA | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr7 | 151359776 | ||||||
chr7:151359911 | C | T | 76 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(73): Show |
88 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.694-230C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151359911 | |||||||
chr7:151360061 | T | C | 25 | a0001c0001t0002g0249 a0001c0001t0003g0206 a0001c0001t0003g0274 others(22): Show |
26 | HG00280.hp2 HG00597.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.694-80T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151360061 | |||||||
chr7:151360096 | A | G | 2 | a0001c0001t0003g0202 a0001c0001t0003g0313 |
2 | HG02055.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.694-45A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151360096 | |||||||
chr7:151360129 | A | G | 1 | a0011c0009t0009g0071 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.694-12A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151360129 | |||||||
chr7:151360130 | T | A | 1 | a0011c0009t0009g0071 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.694-11T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151360130 | |||||||
chr7:151360136 | C | T | 1 | a0011c0009t0009g0071 | 1 | NA19003.hp1 | splice_region_variant&intron_variant | LOW | c.694-5C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 7/14 | chr7 | 151360136 | |||||||
chr7:151360310 | AC | A | 93 | a0001c0002t0001g0004 a0001c0002t0001g0017 a0001c0002t0001g0025 others(90): Show |
98 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.800+66delC | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151360310 | ||||||
chr7:151360386 | T | G | 2 | a0001c0001t0002g0140 a0001c0001t0002g0200 |
2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.800+139T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360386 | |||||||
chr7:151360468 | C | T | 2 | a0001c0002t0001g0095 a0001c0002t0001g0197 |
2 | NA18961.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.800+221C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360468 | |||||||
chr7:151360492 | T | C | 2 | a0001c0005t0001g0184 a0001c0005t0001g0276 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.800+245T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360492 | |||||||
chr7:151360502 | C | T | 1 | a0001c0001t0004g0344 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.800+255C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360502 | |||||||
chr7:151360532 | G | T | 1 | a0001c0003t0003g0337 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.800+285G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360532 | |||||||
chr7:151360557 | A | T | 7 | a0001c0001t0003g0202 a0001c0001t0003g0313 a0001c0001t0006g0008 others(4): Show |
12 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.800+310A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360557 | |||||||
chr7:151360599 | A | G | 80 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(77): Show |
92 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.800+352A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360599 | |||||||
chr7:151360616 | C | A | 2 | a0001c0002t0001g0169 a0010c0013t0001g0170 |
2 | NA18954.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.800+369C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360616 | |||||||
chr7:151360628 | A | AT | 53 | a0001c0001t0002g0140 a0001c0001t0002g0200 a0001c0001t0003g0018 others(50): Show |
62 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.800+389dupT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151360628 | ||||||
chr7:151360756 | TCACAGGT others(9): Show |
T | 5 | a0001c0001t0007g0107 a0001c0001t0007g0132 a0001c0001t0007g0145 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.800+528_800+543del others(16): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151360756 | ||||||
chr7:151360848 | A | G | 316 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(313): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.800+601A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360848 | |||||||
chr7:151360895 | TCAAAGTG others(137): Show |
T | 251 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(248): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(271): Show |
intron_variant | MODIFIER | c.800+660_800+803del | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151360895 | ||||||
chr7:151360907 | T | G | 1 | a0001c0001t0004g0177 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.800+660T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360907 | |||||||
chr7:151360907 | TATTACAG others(137): Show |
T | 1 | a0001c0002t0001g0146 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.800+675_800+818del | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151360907 | ||||||
chr7:151360934 | C | CT | 8 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0268 others(5): Show |
8 | HG00735.hp2 HG01884.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.800+710dupT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151360934 | ||||||
chr7:151360934 | CT | C | 18 | a0001c0001t0002g0167 a0001c0001t0003g0023 a0001c0001t0003g0202 others(15): Show |
24 | HG01069.hp2 HG01074.hp1 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.800+710delT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151360934 | ||||||
chr7:151360975 | C | T | 8 | a0001c0001t0002g0039 a0001c0001t0003g0202 a0001c0001t0003g0313 others(5): Show |
13 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.800+728C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151360975 | |||||||
chr7:151361070 | C | T | 6 | a0001c0001t0003g0345 a0001c0001t0007g0107 a0001c0001t0007g0132 others(3): Show |
6 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.800+823C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151361070 | |||||||
chr7:151361153 | C | A | 1 | a0001c0003t0005g0364 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.800+906C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151361153 | |||||||
chr7:151361159 | G | A | 1 | a0001c0001t0005g0369 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.800+912G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151361159 | |||||||
chr7:151361537 | A | T | 254 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(251): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.800+1290A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151361537 | |||||||
chr7:151361563 | G | A | 1 | a0001c0001t0002g0250 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.800+1316G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151361563 | |||||||
chr7:151361645 | A | C | 3 | a0001c0001t0002g0287 a0001c0001t0002g0315 a0001c0001t0002g0316 |
3 | HG02895.hp1 HG03540.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.800+1398A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151361645 | |||||||
chr7:151361688 | T | C | 1 | a0001c0001t0002g0039 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.800+1441T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151361688 | |||||||
chr7:151361739 | T | C | 1 | a0006c0011t0003g0189 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.800+1492T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151361739 | |||||||
chr7:151361770 | C | T | 1 | a0001c0002t0001g0172 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.800+1523C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151361770 | |||||||
chr7:151361838 | A | G | 5 | a0001c0001t0007g0107 a0001c0001t0007g0132 a0001c0001t0007g0145 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.800+1591A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151361838 | |||||||
chr7:151362040 | C | T | 1 | a0001c0003t0002g0328 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.800+1793C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362040 | |||||||
chr7:151362131 | T | C | 312 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(309): Show |
344 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(341): Show |
intron_variant | MODIFIER | c.800+1884T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362131 | |||||||
chr7:151362311 | G | T | 2 | a0001c0001t0003g0202 a0001c0001t0003g0313 |
2 | HG02055.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.800+2064G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362311 | |||||||
chr7:151362353 | T | C | 1 | a0001c0001t0004g0156 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.800+2106T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362353 | |||||||
chr7:151362404 | C | A | 1 | a0001c0002t0001g0325 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.800+2157C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362404 | |||||||
chr7:151362446 | T | C | 52 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0275 others(49): Show |
57 | HG00099.hp1 HG00099.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.800+2199T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362446 | |||||||
chr7:151362451 | G | C | 1 | a0001c0001t0002g0002 | 3 | HG01081.hp1 HG01109.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.800+2204G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362451 | |||||||
chr7:151362517 | T | C | 8 | a0001c0001t0002g0043 a0001c0001t0002g0147 a0001c0001t0002g0154 others(5): Show |
8 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.800+2270T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362517 | |||||||
chr7:151362575 | A | T | 1 | a0001c0001t0003g0029 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.800+2328A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362575 | |||||||
chr7:151362648 | G | T | 75 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(72): Show |
87 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.800+2401G>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362648 | |||||||
chr7:151362707 | A | C | 53 | a0001c0001t0002g0140 a0001c0001t0002g0200 a0001c0001t0003g0018 others(50): Show |
62 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.800+2460A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362707 | |||||||
chr7:151362803 | A | G | 31 | a0001c0002t0001g0010 a0001c0002t0001g0048 a0001c0002t0001g0069 others(28): Show |
32 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(29): Show |
intron_variant | MODIFIER | c.800+2556A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362803 | |||||||
chr7:151362855 | C | T | 50 | a0001c0001t0003g0018 a0001c0001t0003g0034 a0001c0001t0003g0180 others(47): Show |
59 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(56): Show |
intron_variant | MODIFIER | c.800+2608C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362855 | |||||||
chr7:151362988 | C | T | 254 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(251): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.800+2741C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151362988 | |||||||
chr7:151363182 | T | C | 5 | a0001c0001t0007g0107 a0001c0001t0007g0132 a0001c0001t0007g0145 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.800+2935T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151363182 | |||||||
chr7:151363417 | G | A | 7 | a0001c0001t0003g0202 a0001c0001t0003g0313 a0001c0001t0006g0008 others(4): Show |
12 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.800+3170G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151363417 | |||||||
chr7:151363453 | T | TA | 59 | a0001c0001t0002g0039 a0001c0001t0002g0043 a0001c0001t0002g0140 others(56): Show |
68 | HG00423.hp1 HG01069.hp2 HG01070.hp1 others(65): Show |
intron_variant | MODIFIER | c.800+3221dupA | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151363453 | ||||||
chr7:151363453 | T | TAAAA | 7 | a0001c0001t0003g0202 a0001c0001t0003g0313 a0001c0001t0006g0008 others(4): Show |
12 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.800+3218_800+3221d others(6): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151363453 | ||||||
chr7:151363453 | TA | T | 93 | a0001c0001t0002g0272 a0001c0002t0001g0004 a0001c0002t0001g0017 others(90): Show |
98 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.800+3221delA | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151363453 | ||||||
chr7:151363634 | A | T | 2 | a0001c0001t0002g0140 a0001c0001t0002g0200 |
2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.801-3305A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151363634 | |||||||
chr7:151363721 | T | C | 1 | a0001c0002t0001g0304 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.801-3218T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151363721 | |||||||
chr7:151363751 | GAA | G | 7 | a0001c0001t0003g0202 a0001c0001t0003g0313 a0001c0001t0006g0008 others(4): Show |
12 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.801-3183_801-3182d others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151363751 | ||||||
chr7:151363756 | AAGTT | A | 53 | a0001c0001t0002g0140 a0001c0001t0002g0200 a0001c0001t0003g0018 others(50): Show |
62 | HG00423.hp1 HG00735.hp2 HG01069.hp1 others(59): Show |
intron_variant | MODIFIER | c.801-3180_801-3177d others(6): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151363756 | ||||||
chr7:151363954 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.801-2985C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151363954 | |||||||
chr7:151364019 | C | T | 2 | a0001c0001t0002g0140 a0001c0001t0002g0200 |
2 | HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.801-2920C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364019 | |||||||
chr7:151364051 | C | A | 5 | a0001c0001t0007g0107 a0001c0001t0007g0132 a0001c0001t0007g0145 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.801-2888C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364051 | |||||||
chr7:151364081 | A | C | 3 | a0001c0001t0003g0034 a0001c0001t0003g0277 a0001c0001t0003g0326 |
3 | HG02280.hp2 HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.801-2858A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364081 | |||||||
chr7:151364084 | G | A | 9 | a0001c0001t0002g0043 a0001c0001t0002g0147 a0001c0001t0002g0154 others(6): Show |
9 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.801-2855G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364084 | |||||||
chr7:151364144 | C | T | 1 | a0001c0002t0001g0017 | 2 | NA18949.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.801-2795C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364144 | |||||||
chr7:151364290 | A | G | 312 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(309): Show |
349 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.801-2649A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364290 | |||||||
chr7:151364349 | A | AG | 7 | a0001c0001t0003g0202 a0001c0001t0003g0313 a0001c0001t0006g0008 others(4): Show |
12 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.801-2588dupG | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151364349 | ||||||
chr7:151364397 | G | C | 5 | a0001c0001t0004g0037 a0001c0001t0004g0343 a0001c0001t0004g0344 others(2): Show |
5 | HG02486.hp1 HG02717.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.801-2542G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364397 | |||||||
chr7:151364432 | CA | C | 219 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0043 others(216): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.801-2498delA | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151364432 | ||||||
chr7:151364440 | A | AC | 4 | a0001c0001t0002g0015 a0001c0001t0002g0058 a0001c0001t0002g0131 others(1): Show |
5 | NA18940.hp2 NA18946.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.801-2499_801-2498i others(3): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364440 | |||||||
chr7:151364441 | A | C | 91 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(88): Show |
107 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.801-2498A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364441 | |||||||
chr7:151364442 | C | A | 90 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(87): Show |
102 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(99): Show |
intron_variant | MODIFIER | c.801-2497C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364442 | |||||||
chr7:151364452 | A | C | 4 | a0001c0001t0002g0039 a0001c0001t0003g0180 a0001c0001t0003g0181 others(1): Show |
4 | HG02615.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.801-2487A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364452 | |||||||
chr7:151364453 | A | C | 304 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(301): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(337): Show |
intron_variant | MODIFIER | c.801-2486A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364453 | |||||||
chr7:151364465 | T | G | 3 | a0001c0001t0003g0034 a0001c0001t0003g0277 a0001c0001t0003g0326 |
3 | HG02280.hp2 HG02647.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.801-2474T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364465 | |||||||
chr7:151364481 | A | C | 313 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(310): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(342): Show |
intron_variant | MODIFIER | c.801-2458A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364481 | |||||||
chr7:151364556 | G | C | 1 | a0001c0001t0004g0324 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.801-2383G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364556 | |||||||
chr7:151364867 | T | C | 316 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(313): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.801-2072T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364867 | |||||||
chr7:151364872 | C | T | 1 | a0001c0002t0001g0281 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.801-2067C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364872 | |||||||
chr7:151364908 | G | A | 1 | a0001c0002t0001g0077 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.801-2031G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364908 | |||||||
chr7:151364974 | A | AAATTTTT others(317): Show |
1 | a0001c0001t0004g0324 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.801-1952_801-1951i others(326): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151364974 | ||||||
chr7:151364984 | T | A | 1 | a0011c0009t0009g0071 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.801-1955T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151364984 | |||||||
chr7:151364992 | AT | A | 8 | a0001c0001t0003g0202 a0001c0001t0003g0313 a0001c0001t0003g0355 others(5): Show |
13 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(10): Show |
intron_variant | MODIFIER | c.801-1935delT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151364992 | ||||||
chr7:151365030 | T | C | 321 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(318): Show |
353 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(350): Show |
intron_variant | MODIFIER | c.801-1909T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365030 | |||||||
chr7:151365076 | G | A | 2 | a0001c0001t0003g0338 a0001c0001t0005g0363 |
2 | HG01099.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.801-1863G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365076 | |||||||
chr7:151365078 | C | A | 21 | a0001c0001t0003g0018 a0001c0001t0003g0188 a0001c0001t0003g0210 others(18): Show |
26 | HG00423.hp1 HG01884.hp1 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.801-1861C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365078 | |||||||
chr7:151365093 | A | G | 316 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(313): Show |
348 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(345): Show |
intron_variant | MODIFIER | c.801-1846A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365093 | |||||||
chr7:151365210 | T | G | 5 | a0001c0001t0007g0107 a0001c0001t0007g0132 a0001c0001t0007g0145 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.801-1729T>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365210 | |||||||
chr7:151365262 | G | A | 95 | a0001c0002t0001g0004 a0001c0002t0001g0017 a0001c0002t0001g0025 others(92): Show |
100 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.801-1677G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365262 | |||||||
chr7:151365318 | CT | C | 298 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(295): Show |
329 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(326): Show |
intron_variant | MODIFIER | c.801-1607delT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151365318 | ||||||
chr7:151365434 | G | A | 7 | a0001c0002t0001g0010 a0001c0002t0001g0069 a0001c0002t0001g0094 others(4): Show |
8 | NA18956.hp2 NA18970.hp2 NA18975.hp1 others(5): Show |
intron_variant | MODIFIER | c.801-1505G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365434 | |||||||
chr7:151365551 | T | C | 1 | a0001c0001t0002g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.801-1388T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365551 | |||||||
chr7:151365669 | C | T | 5 | a0001c0001t0007g0107 a0001c0001t0007g0132 a0001c0001t0007g0145 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.801-1270C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365669 | |||||||
chr7:151365707 | G | A | 1 | a0001c0003t0002g0105 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.801-1232G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365707 | |||||||
chr7:151365714 | A | G | 5 | a0001c0002t0001g0152 a0001c0002t0001g0299 a0001c0002t0001g0307 others(2): Show |
5 | HG00738.hp1 HG02145.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.801-1225A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365714 | |||||||
chr7:151365745 | G | A | 1 | a0001c0001t0002g0039 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.801-1194G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365745 | |||||||
chr7:151365766 | G | A | 1 | a0001c0002t0001g0031 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.801-1173G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365766 | |||||||
chr7:151365890 | C | CT | 252 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(249): Show |
275 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.801-1039dupT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151365890 | ||||||
chr7:151365890 | CT | C | 24 | a0001c0001t0002g0287 a0001c0001t0002g0315 a0001c0001t0002g0316 others(21): Show |
29 | HG00423.hp1 HG01884.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.801-1039delT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151365890 | ||||||
chr7:151365905 | C | A | 4 | a0001c0001t0004g0011 a0001c0001t0004g0049 a0001c0001t0004g0099 others(1): Show |
5 | HG02132.hp2 NA18941.hp2 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.801-1034C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365905 | |||||||
chr7:151365910 | A | G | 1 | a0001c0001t0003g0212 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.801-1029A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151365910 | |||||||
chr7:151366245 | A | T | 1 | a0001c0001t0004g0028 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.801-694A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151366245 | |||||||
chr7:151366404 | G | C | 1 | a0001c0001t0004g0032 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.801-535G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151366404 | |||||||
chr7:151366471 | C | A | 2 | a0001c0001t0003g0180 a0001c0001t0003g0181 |
2 | HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.801-468C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151366471 | |||||||
chr7:151366478 | A | G | 5 | a0001c0001t0007g0107 a0001c0001t0007g0132 a0001c0001t0007g0145 others(2): Show |
5 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.801-461A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151366478 | |||||||
chr7:151366519 | T | TAAAG | 3 | a0001c0001t0002g0039 a0001c0001t0003g0158 a0001c0001t0003g0330 |
3 | HG02965.hp2 HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.801-397_801-394dup others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151366519 | ||||||
chr7:151366519 | TAAAG | T | 325 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(322): Show |
362 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(359): Show |
intron_variant | MODIFIER | c.801-397_801-394del others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr7 | 151366519 | ||||||
chr7:151366547 | G | A | 8 | a0001c0001t0002g0043 a0001c0001t0002g0147 a0001c0001t0002g0154 others(5): Show |
8 | HG01069.hp2 HG01070.hp1 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.801-392G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151366547 | |||||||
chr7:151366708 | C | A | 6 | a0001c0001t0004g0024 a0001c0001t0004g0258 a0001c0001t0004g0266 others(3): Show |
7 | HG01074.hp1 HG01243.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.801-231C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151366708 | |||||||
chr7:151366783 | C | G | 1 | a0001c0003t0003g0336 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.801-156C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 8/14 | chr7 | 151366783 | |||||||
chr7:151367188 | T | A | 2 | a0001c0005t0001g0184 a0001c0005t0001g0276 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.987+63T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 9/14 | chr7 | 151367188 | |||||||
chr7:151367219 | A | G | 334 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(331): Show |
371 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(368): Show |
intron_variant | MODIFIER | c.987+94A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 9/14 | chr7 | 151367219 | |||||||
chr7:151367336 | A | G | 148 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0054 others(145): Show |
157 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.987+211A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 9/14 | chr7 | 151367336 | |||||||
chr7:151367645 | A | T | 1 | a0001c0002t0001g0123 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.988-216A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 9/14 | chr7 | 151367645 | |||||||
chr7:151367646 | C | T | 16 | a0001c0001t0003g0034 a0001c0001t0003g0277 a0001c0001t0003g0326 others(13): Show |
19 | HG01074.hp1 HG01243.hp2 HG01255.hp1 others(16): Show |
intron_variant | MODIFIER | c.988-215C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 9/14 | chr7 | 151367646 | |||||||
chr7:151367672 | A | G | 3 | a0001c0001t0002g0174 a0001c0001t0002g0176 a0001c0004t0001g0175 |
3 | HG01496.hp2 HG01943.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.988-189A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 9/14 | chr7 | 151367672 | |||||||
chr7:151367786 | A | G | 119 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(116): Show |
139 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.988-75A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 9/14 | chr7 | 151367786 | |||||||
chr7:151368127 | G | C | 4 | a0001c0001t0004g0028 a0001c0001t0004g0324 a0001c0001t0008g0201 others(1): Show |
5 | HG02647.hp1 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1095+159G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 10/14 | chr7 | 151368127 | |||||||
chr7:151368388 | C | T | 1 | a0001c0002t0001g0194 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.1096-347C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 10/14 | chr7 | 151368388 | |||||||
chr7:151368590 | A | G | 1 | a0001c0002t0001g0017 | 2 | NA18949.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1096-145A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 10/14 | chr7 | 151368590 | |||||||
chr7:151368992 | GA | G | 6 | a0001c0001t0007g0107 a0001c0001t0007g0132 a0001c0001t0007g0145 others(3): Show |
6 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1248+107delA | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 151368992 | ||||||
chr7:151369071 | G | A | 2 | a0001c0001t0003g0210 a0005c0010t0003g0209 |
2 | HG01884.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1248+184G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151369071 | |||||||
chr7:151369455 | T | C | 134 | a0001c0001t0003g0033 a0001c0001t0003g0136 a0001c0001t0003g0259 others(131): Show |
140 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.1248+568T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151369455 | |||||||
chr7:151369649 | A | G | 1 | a0001c0001t0002g0065 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1248+762A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151369649 | |||||||
chr7:151369790 | A | G | 1 | a0001c0001t0007g0145 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1248+903A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151369790 | |||||||
chr7:151370028 | C | T | 7 | a0001c0001t0003g0202 a0001c0001t0003g0313 a0001c0001t0006g0008 others(4): Show |
12 | HG02055.hp1 HG02258.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.1248+1141C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151370028 | |||||||
chr7:151370084 | G | C | 2 | a0001c0001t0002g0055 a0001c0001t0002g0137 |
2 | HG01257.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1248+1197G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151370084 | |||||||
chr7:151370097 | CT | C | 15 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0043 others(12): Show |
18 | HG01069.hp2 HG01070.hp1 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.1248+1224delT | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 151370097 | ||||||
chr7:151370165 | C | G | 2 | a0001c0001t0008g0201 a0001c0001t0008g0203 |
2 | HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1248+1278C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151370165 | |||||||
chr7:151370392 | A | C | 1 | a0001c0001t0007g0256 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1248+1505A>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151370392 | |||||||
chr7:151370503 | A | T | 259 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(256): Show |
283 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.1248+1616A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151370503 | |||||||
chr7:151370692 | C | G | 111 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(108): Show |
129 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.1248+1805C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151370692 | |||||||
chr7:151371146 | C | T | 2 | a0001c0001t0003g0044 a0001c0001t0003g0157 |
2 | HG03017.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.1248+2259C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151371146 | |||||||
chr7:151371176 | C | T | 327 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(324): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.1248+2289C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151371176 | |||||||
chr7:151371180 | G | A | 1 | a0001c0001t0003g0042 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1248+2293G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151371180 | |||||||
chr7:151371180 | G | C | 3 | a0001c0003t0002g0306 a0001c0003t0002g0334 a0001c0003t0002g0335 |
3 | HG00140.hp2 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1248+2293G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151371180 | |||||||
chr7:151371363 | A | AC | 247 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(244): Show |
271 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.1248+2482dupC | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 151371363 | ||||||
chr7:151371363 | A | ACC | 16 | a0001c0001t0002g0051 a0001c0001t0002g0053 a0001c0001t0002g0088 others(13): Show |
16 | HG01934.hp1 HG02135.hp2 HG02809.hp1 others(13): Show |
intron_variant | MODIFIER | c.1248+2481_1248+248 others(6): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 151371363 | ||||||
chr7:151371554 | G | C | 1 | a0001c0001t0002g0119 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1249-2543G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151371554 | |||||||
chr7:151371647 | C | T | 2 | a0001c0005t0001g0184 a0001c0005t0001g0276 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1249-2450C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151371647 | |||||||
chr7:151371672 | A | T | 1 | a0001c0001t0002g0096 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1249-2425A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151371672 | |||||||
chr7:151371836 | C | T | 8 | a0001c0001t0007g0107 a0001c0001t0007g0132 a0001c0001t0007g0145 others(5): Show |
8 | HG02572.hp1 HG02622.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1249-2261C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151371836 | |||||||
chr7:151371843 | C | T | 1 | a0001c0002t0001g0339 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1249-2254C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151371843 | |||||||
chr7:151372043 | T | A | 2 | a0001c0002t0001g0299 a0001c0002t0001g0307 |
2 | HG02559.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1249-2054T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372043 | |||||||
chr7:151372138 | C | T | 1 | a0001c0001t0002g0102 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1249-1959C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372138 | |||||||
chr7:151372170 | A | G | 2 | a0001c0001t0008g0201 a0001c0001t0008g0203 |
2 | HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1249-1927A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372170 | |||||||
chr7:151372210 | A | G | 77 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(74): Show |
89 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.1249-1887A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372210 | |||||||
chr7:151372221 | C | A | 2 | a0001c0001t0008g0201 a0001c0001t0008g0203 |
2 | HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1249-1876C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372221 | |||||||
chr7:151372243 | C | T | 5 | a0001c0002t0001g0149 a0001c0002t0001g0153 a0001c0002t0001g0234 others(2): Show |
5 | HG00639.hp1 HG00741.hp1 HG01123.hp2 others(2): Show |
intron_variant | MODIFIER | c.1249-1854C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372243 | |||||||
chr7:151372325 | T | C | 250 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(247): Show |
274 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.1249-1772T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372325 | |||||||
chr7:151372608 | A | G | 264 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(261): Show |
288 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(285): Show |
intron_variant | MODIFIER | c.1249-1489A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372608 | |||||||
chr7:151372648 | G | A | 2 | a0001c0002t0001g0236 a0001c0002t0001g0238 |
2 | HG02074.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.1249-1449G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372648 | |||||||
chr7:151372773 | G | A | 10 | a0001c0001t0007g0107 a0001c0001t0007g0132 a0001c0001t0007g0145 others(7): Show |
10 | HG02572.hp1 HG02622.hp1 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1249-1324G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372773 | |||||||
chr7:151372900 | C | T | 1 | a0001c0002t0001g0031 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1249-1197C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372900 | |||||||
chr7:151372926 | G | A | 1 | a0005c0010t0003g0209 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1249-1171G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151372926 | |||||||
chr7:151373121 | G | A | 4 | a0001c0001t0002g0051 a0001c0001t0002g0083 a0001c0001t0002g0155 others(1): Show |
4 | HG00323.hp2 HG01934.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1249-976G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151373121 | |||||||
chr7:151373144 | T | C | 4 | a0001c0002t0001g0061 a0001c0002t0001g0120 a0001c0002t0001g0126 others(1): Show |
4 | NA18969.hp2 NA18971.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.1249-953T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151373144 | |||||||
chr7:151373207 | T | C | 142 | a0001c0001t0003g0033 a0001c0001t0003g0136 a0001c0001t0003g0180 others(139): Show |
148 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(145): Show |
intron_variant | MODIFIER | c.1249-890T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151373207 | |||||||
chr7:151373445 | C | T | 133 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0259 others(130): Show |
139 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.1249-652C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151373445 | |||||||
chr7:151373602 | G | A | 1 | a0001c0002t0001g0252 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1249-495G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151373602 | |||||||
chr7:151373657 | T | C | 1 | a0001c0001t0003g0135 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1249-440T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151373657 | |||||||
chr7:151373702 | G | A | 5 | a0001c0002t0001g0148 a0001c0002t0001g0289 a0001c0002t0001g0290 others(2): Show |
5 | HG00639.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1249-395G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | chr7 | 151373702 | |||||||
chr7:151373911 | ACC | A | 4 | a0001c0001t0003g0206 a0001c0001t0003g0210 a0001c0001t0003g0274 others(1): Show |
4 | HG01884.hp1 HG02055.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1249-183_1249-182d others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr7 | 151373911 | ||||||
chr7:151374257 | C | T | 1 | a0001c0002t0001g0126 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1395+14C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374257 | |||||||
chr7:151374373 | C | G | 1 | a0001c0001t0002g0200 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1395+130C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374373 | |||||||
chr7:151374429 | C | A | 1 | a0001c0001t0004g0373 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1395+186C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374429 | |||||||
chr7:151374540 | G | A | 1 | a0001c0001t0003g0181 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1395+297G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374540 | |||||||
chr7:151374548 | C | T | 1 | a0001c0003t0003g0336 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1395+305C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374548 | |||||||
chr7:151374558 | G | A | 1 | a0001c0002t0001g0017 | 2 | NA18949.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1395+315G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374558 | |||||||
chr7:151374652 | C | A | 14 | a0001c0001t0003g0206 a0001c0001t0003g0210 a0001c0001t0003g0274 others(11): Show |
14 | HG01884.hp1 HG02055.hp2 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1395+409C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374652 | |||||||
chr7:151374753 | T | A | 96 | a0001c0002t0001g0004 a0001c0002t0001g0017 a0001c0002t0001g0025 others(93): Show |
101 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(98): Show |
intron_variant | MODIFIER | c.1395+510T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374753 | |||||||
chr7:151374796 | C | T | 2 | a0001c0005t0001g0184 a0001c0005t0001g0276 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1395+553C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374796 | |||||||
chr7:151374797 | G | A | 2 | a0001c0001t0002g0055 a0001c0001t0002g0137 |
2 | HG01257.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.1395+554G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374797 | |||||||
chr7:151374801 | C | T | 1 | a0001c0001t0004g0037 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1395+558C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374801 | |||||||
chr7:151374840 | C | T | 125 | a0001c0002t0001g0004 a0001c0002t0001g0010 a0001c0002t0001g0017 others(122): Show |
131 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(128): Show |
intron_variant | MODIFIER | c.1395+597C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374840 | |||||||
chr7:151374852 | T | A | 2 | a0001c0005t0001g0184 a0001c0005t0001g0276 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1395+609T>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374852 | |||||||
chr7:151374885 | A | G | 259 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(256): Show |
283 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.1395+642A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374885 | |||||||
chr7:151374962 | G | A | 2 | a0001c0005t0001g0184 a0001c0005t0001g0276 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1395+719G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374962 | |||||||
chr7:151374978 | A | G | 327 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(324): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.1395+735A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151374978 | |||||||
chr7:151375010 | T | C | 2 | a0001c0005t0001g0184 a0001c0005t0001g0276 |
2 | HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1395+767T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375010 | |||||||
chr7:151375022 | G | A | 6 | a0001c0001t0007g0107 a0001c0001t0007g0132 a0001c0001t0007g0145 others(3): Show |
6 | HG02572.hp1 HG02622.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1395+779G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375022 | |||||||
chr7:151375159 | C | T | 1 | a0001c0001t0004g0049 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1396-689C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375159 | |||||||
chr7:151375198 | A | T | 3 | a0001c0001t0002g0140 a0001c0001t0002g0200 a0001c0003t0002g0036 |
3 | HG01109.hp1 HG01243.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1396-650A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375198 | |||||||
chr7:151375254 | C | T | 327 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0002 others(324): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(360): Show |
intron_variant | MODIFIER | c.1396-594C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375254 | |||||||
chr7:151375279 | T | C | 12 | a0001c0001t0001g0365 a0001c0001t0002g0001 a0001c0001t0002g0043 others(9): Show |
15 | HG01069.hp2 HG01070.hp1 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1396-569T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375279 | |||||||
chr7:151375326 | A | G | 1 | a0001c0002t0001g0164 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1396-522A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375326 | |||||||
chr7:151375475 | C | A | 1 | a0001c0001t0003g0259 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1396-373C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375475 | |||||||
chr7:151375588 | C | T | 2 | a0001c0004t0001g0117 a0001c0004t0001g0215 |
2 | NA19012.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1396-260C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375588 | |||||||
chr7:151375792 | TCTGA | T | 4 | a0001c0001t0002g0039 a0001c0001t0002g0287 a0001c0001t0002g0315 others(1): Show |
4 | HG02895.hp1 HG02965.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1396-55_1396-52del others(4): Show |
NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375792 | |||||||
chr7:151375793 | C | G | 1 | a0001c0001t0004g0352 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1396-55C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 12/14 | chr7 | 151375793 | |||||||
chr7:151376007 | C | T | 67 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(64): Show |
77 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(74): Show |
intron_variant | MODIFIER | c.1491+64C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376007 | |||||||
chr7:151376035 | A | T | 5 | a0001c0001t0003g0180 a0001c0001t0003g0181 a0001c0001t0003g0268 others(2): Show |
5 | HG00735.hp2 HG01884.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1491+92A>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376035 | |||||||
chr7:151376148 | G | A | 7 | a0001c0001t0007g0107 a0001c0001t0007g0132 a0001c0001t0007g0145 others(4): Show |
7 | HG02486.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1491+205G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376148 | |||||||
chr7:151376312 | A | G | 4 | a0001c0001t0003g0210 a0001c0002t0001g0261 a0001c0002t0001g0262 others(1): Show |
4 | HG01884.hp1 HG02055.hp2 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1492-322A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376312 | |||||||
chr7:151376438 | C | A | 4 | a0001c0001t0002g0140 a0001c0001t0002g0287 a0001c0001t0002g0316 others(1): Show |
4 | HG01243.hp1 HG02895.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1492-196C>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376438 | |||||||
chr7:151376484 | T | C | 7 | a0001c0001t0007g0107 a0001c0001t0007g0132 a0001c0001t0007g0145 others(4): Show |
7 | HG02486.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1492-150T>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376484 | |||||||
chr7:151376568 | A | G | 5 | a0001c0001t0006g0008 a0001c0001t0006g0009 a0001c0001t0006g0026 others(2): Show |
10 | HG02258.hp2 HG02630.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1492-66A>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376568 | |||||||
chr7:151376572 | C | G | 117 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(114): Show |
130 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1492-62C>G | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376572 | |||||||
chr7:151376576 | C | T | 11 | a0001c0002t0001g0010 a0001c0002t0001g0069 a0001c0002t0001g0094 others(8): Show |
12 | NA18947.hp2 NA18951.hp2 NA18956.hp2 others(9): Show |
intron_variant | MODIFIER | c.1492-58C>T | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376576 | |||||||
chr7:151376577 | G | A | 2 | a0001c0002t0001g0074 a0001c0002t0001g0146 |
2 | HG02027.hp1 HG02040.hp1 |
intron_variant | MODIFIER | c.1492-57G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376577 | |||||||
chr7:151376578 | G | A | 3 | a0001c0001t0003g0210 a0001c0001t0003g0274 a0005c0010t0003g0209 |
3 | HG01884.hp1 HG02055.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1492-56G>A | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 13/14 | chr7 | 151376578 | |||||||
chr7:151376929 | G | C | 130 | a0001c0001t0004g0286 a0001c0001t0004g0327 a0001c0001t0004g0354 others(127): Show |
136 | HG00099.hp2 HG00408.hp1 HG00609.hp1 others(133): Show |
intron_variant | MODIFIER | c.1669+118G>C | NUB1 | ENSG00000013374.17 | transcript | ENST00000568733.6 | protein_coding | 14/14 | chr7 | 151376929 |