Item | Value |
---|---|
geneid | 8729 |
ensemblid | ENSG00000107862.7 |
hgncid | 4181 |
symbol | GBF1 |
name | golgi brefeldin A resistant guanine nucleotide exchange factor 1 |
refseq_nuc | NM_001377137.1 |
refseq_prot | NP_001364066.1 |
ensembl_nuc | ENST00000369983.5 |
ensembl_prot | ENSP00000359000.4 |
mane_status | MANE Select |
chr | chr10 |
start | 102245532 |
end | 102382896 |
strand | + |
ver | v1.2 |
region | chr10:102245532-102382896 |
region5000 | chr10:102240532-102387896 |
regionname0 | GBF1_chr10_102245532_102382896 |
regionname5000 | GBF1_chr10_102240532_102387896 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1860 | 300 | 81 | 53 | 122 | 9 | 33 | 97 | GBF1_chr10_102240532_102387896 | GBF1 | MVDKN others(1855): Show |
chr10 | 102240532 | 102387896 |
a0002 | 0/0 | 1860 | 12 | 0 | 7 | 2 | 3 | 0 | 2 | GBF1_chr10_102240532_102387896 | GBF1 | MVDKN others(1855): Show |
chr10 | 102240532 | 102387896 |
a0003 | 0/0 | 1860 | 5 | 0 | 0 | 5 | 0 | 0 | 4 | GBF1_chr10_102240532_102387896 | GBF1 | MVDKN others(1855): Show |
chr10 | 102240532 | 102387896 |
a0004 | 0/0 | 1860 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | GBF1_chr10_102240532_102387896 | GBF1 | MVDKN others(1855): Show |
chr10 | 102240532 | 102387896 |
a0005 | 0/0 | 1860 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | MVDKN others(1855): Show |
chr10 | 102240532 | 102387896 |
a0006 | 0/0 | 1860 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | MVDKN others(1855): Show |
chr10 | 102240532 | 102387896 |
a0007 | 0/0 | 1860 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | MVDKN others(1855): Show |
chr10 | 102240532 | 102387896 |
a0008 | 0/0 | 1860 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | MVDKN others(1855): Show |
chr10 | 102240532 | 102387896 |
a0009 | 0/0 | 1860 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | MVDKN others(1855): Show |
chr10 | 102240532 | 102387896 |
a0010 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | MVDKN others(1855): Show |
chr10 | 102240532 | 102387896 |
a0011 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | MVDKN others(1855): Show |
chr10 | 102240532 | 102387896 |
a0012 | 0/0 | 1860 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | MVDKN others(1855): Show |
chr10 | 102240532 | 102387896 |
a0013 | 0/0 | 1860 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | MVDKN others(1855): Show |
chr10 | 102240532 | 102387896 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 5580 | 274 | 67 | 49 | 120 | 8 | 29 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0001c0003 | 0/0 | 5580 | 11 | 6 | 1 | 0 | 1 | 3 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0001c0004 | 0/0 | 5580 | 6 | 6 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0001c0007 | 1/0 | 5580 | 2 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0001c0013 | 0/0 | 5580 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0001c0014 | 0/0 | 5580 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0001c0016 | 0/0 | 5580 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0001c0021 | 0/0 | 5580 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0001c0022 | 0/0 | 5580 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0001c0023 | 0/0 | 5580 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0001c0024 | 0/0 | 5580 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0002c0002 | 0/0 | 5580 | 12 | 0 | 7 | 2 | 3 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0003c0005 | 0/0 | 5580 | 5 | 0 | 0 | 5 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0004c0008 | 0/0 | 5580 | 2 | 0 | 0 | 2 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0004c0020 | 0/0 | 5580 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0005c0006 | 0/0 | 5580 | 2 | 0 | 0 | 2 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0006c0015 | 0/0 | 5580 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0007c0011 | 0/0 | 5580 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0008c0018 | 0/0 | 5580 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0009c0019 | 0/0 | 5580 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0010c0012 | 0/0 | 5580 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0011c0010 | 0/0 | 5580 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0012c0017 | 0/0 | 5580 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 | ||
a0013c0009 | 0/0 | 5580 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | ATGGT others(5575): Show |
chr10 | 102240532 | 102387896 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6403 | 124 | 54 | 18 | 42 | 3 | 7 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0001c0001t0002 | 0/1 | 6403 | 80 | 10 | 19 | 35 | 3 | 12 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0001c0001t0003 | 0/0 | 6403 | 65 | 2 | 12 | 42 | 1 | 8 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0001c0001t0005 | 0/0 | 6403 | 2 | 1 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0001c0001t0006 | 0/0 | 6403 | 2 | 0 | 0 | 0 | 0 | 2 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0001c0001t0007 | 0/0 | 6403 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0001c0003t0001 | 0/0 | 6403 | 11 | 6 | 1 | 0 | 1 | 3 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0001c0004t0002 | 0/0 | 6403 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0001c0004t0004 | 0/0 | 6403 | 5 | 5 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0001c0007t0001 | 0/0 | 6403 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0001c0007t0002 | 1/0 | 6403 | 1 | 0 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0001c0013t0002 | 0/0 | 6403 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0001c0014t0001 | 0/0 | 6403 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0001c0016t0001 | 0/0 | 6403 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0001c0021t0004 | 0/0 | 6403 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0001c0022t0003 | 0/0 | 6403 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0001c0023t0003 | 0/0 | 6403 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0001c0024t0001 | 0/0 | 6403 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0002c0002t0001 | 0/0 | 6403 | 12 | 0 | 7 | 2 | 3 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0003c0005t0002 | 0/0 | 6403 | 5 | 0 | 0 | 5 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0004c0008t0001 | 0/0 | 6403 | 2 | 0 | 0 | 2 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0004c0020t0003 | 0/0 | 6403 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0005c0006t0001 | 0/0 | 6403 | 2 | 0 | 0 | 2 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0006c0015t0002 | 0/0 | 6403 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0007c0011t0001 | 0/0 | 6403 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0008c0018t0001 | 0/0 | 6403 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0009c0019t0002 | 0/0 | 6403 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0010c0012t0002 | 0/0 | 6403 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0011c0010t0001 | 0/0 | 6403 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0012c0017t0001 | 0/0 | 6403 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
a0013c0009t0001 | 0/0 | 6403 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | AGTTA others(6398): Show |
chr10 | 102240532 | 102387896 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0069 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0290 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0003g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0005g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0006g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0006g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0001t0007g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0003t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0003t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0003t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0003t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0003t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0003t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0003t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0003t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0003t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0004t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0004t0004g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0004t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0004t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0004t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0007t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0007t0002g0098 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0013t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0014t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0016t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0021t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0022t0003g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0023t0003g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0001c0024t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0002c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0002c0002t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0002c0002t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0002c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0003c0005t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0003c0005t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0003c0005t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0003c0005t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0003c0005t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0004c0008t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0004c0008t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0004c0020t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0005c0006t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0005c0006t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0006c0015t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0007c0011t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0008c0018t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0009c0019t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0010c0012t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0011c0010t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0012c0017t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
a0013c0009t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0290 | EUR | GBR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0037 | EUR | GBR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG00280 | hp1 | a0001 | c0001 | t0005 | g0155 | EUR | FIN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0062 | EUR | FIN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG00544 | hp1 | a0005 | c0006 | t0001 | g0156 | EAS | CHS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | CHS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0233 | EAS | CHS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | CHS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | CHS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0258 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | CHS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0309 | EAS | CHS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0268 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG00735 | hp2 | a0002 | c0002 | t0001 | g0205 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG00738 | hp1 | a0006 | c0015 | t0002 | g0061 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0260 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01070 | hp2 | a0001 | c0003 | t0001 | g0209 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0002 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01074 | hp1 | a0007 | c0011 | t0001 | g0294 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01081 | hp1 | a0001 | c0024 | t0001 | g0228 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0171 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01106 | hp1 | a0001 | c0023 | t0003 | g0269 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01175 | hp1 | a0008 | c0018 | t0001 | g0204 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01192 | hp1 | a0001 | c0013 | t0002 | g0048 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0270 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0243 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0198 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01346 | hp1 | a0001 | c0001 | t0002 | g0013 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0036 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0181 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0272 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0249 | EUR | IBS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | IBS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0107 | EUR | IBS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01516 | hp2 | a0001 | c0003 | t0001 | g0108 | EUR | IBS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0202 | EUR | IBS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0244 | EUR | IBS | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0124 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01928 | hp2 | a0009 | c0019 | t0002 | g0042 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0040 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0043 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0172 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0187 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0265 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02004 | hp1 | a0001 | c0001 | t0003 | g0237 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0288 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02056 | hp1 | a0001 | c0001 | t0003 | g0282 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0087 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02071 | hp1 | a0003 | c0005 | t0002 | g0101 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0302 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02074 | hp1 | a0001 | c0001 | t0003 | g0303 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02080 | hp2 | a0001 | c0001 | t0003 | g0314 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02135 | hp2 | a0005 | c0006 | t0001 | g0157 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0116 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0316 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0027 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02257 | hp1 | a0001 | c0003 | t0001 | g0225 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0239 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0313 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02280 | hp1 | a0001 | c0004 | t0004 | g0001 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0039 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02451 | hp2 | a0001 | c0003 | t0001 | g0226 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0079 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0180 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0257 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02698 | hp2 | a0001 | c0003 | t0001 | g0210 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0057 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0278 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02738 | hp2 | a0001 | c0003 | t0001 | g0221 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02818 | hp2 | a0011 | c0010 | t0001 | g0112 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02895 | hp1 | a0001 | c0003 | t0001 | g0227 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0208 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02965 | hp2 | a0001 | c0004 | t0004 | g0016 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0058 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02976 | hp2 | a0001 | c0003 | t0001 | g0224 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03017 | hp1 | a0012 | c0017 | t0001 | g0192 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03195 | hp1 | a0013 | c0009 | t0001 | g0216 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03209 | hp1 | a0001 | c0007 | t0001 | g0328 | AFR | MSL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | MSL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | MSL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03486 | hp1 | a0001 | c0003 | t0001 | g0206 | AFR | MSL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | MSL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | ESN | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03669 | hp1 | a0001 | c0003 | t0001 | g0211 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0289 | SAS | BEB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | BEB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0046 | SAS | BEB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0264 | SAS | BEB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03927 | hp2 | a0001 | c0001 | t0006 | g0164 | SAS | BEB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0045 | SAS | BEB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | BEB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG04115 | hp1 | a0001 | c0001 | t0003 | g0241 | SAS | STU | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | STU | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0019 | SAS | BEB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | BEB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | STU | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG04204 | hp2 | a0001 | c0001 | t0003 | g0256 | SAS | STU | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG04228 | hp1 | a0001 | c0014 | t0001 | g0166 | SAS | STU | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0259 | SAS | STU | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18522 | hp1 | a0001 | c0004 | t0004 | g0001 | AFR | YRI | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0296 | AFR | YRI | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | YRI | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | YRI | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0271 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0266 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18944 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18949 | hp2 | a0004 | c0008 | t0001 | g0194 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0283 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18951 | hp2 | a0001 | c0001 | t0007 | g0146 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18952 | hp1 | a0003 | c0005 | t0002 | g0076 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0280 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18953 | hp1 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0306 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18957 | hp2 | a0004 | c0008 | t0001 | g0199 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0176 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18963 | hp1 | a0001 | c0001 | t0003 | g0318 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0319 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18967 | hp1 | a0001 | c0001 | t0003 | g0291 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18970 | hp2 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18979 | hp1 | a0001 | c0001 | t0003 | g0284 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0276 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18992 | hp2 | a0003 | c0005 | t0002 | g0078 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18994 | hp1 | a0001 | c0016 | t0001 | g0188 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18994 | hp2 | a0004 | c0020 | t0003 | g0311 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0315 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0285 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0305 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0261 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19007 | hp1 | a0001 | c0022 | t0003 | g0234 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19010 | hp1 | a0003 | c0005 | t0002 | g0077 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | LWK | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19030 | hp2 | a0001 | c0004 | t0004 | g0014 | AFR | LWK | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0207 | AFR | LWK | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0322 | AFR | LWK | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0277 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19057 | hp2 | a0001 | c0001 | t0003 | g0317 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19062 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19063 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19068 | hp2 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0304 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0281 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0287 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19083 | hp1 | a0001 | c0001 | t0003 | g0273 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0312 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19084 | hp2 | a0002 | c0002 | t0001 | g0104 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0007 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0274 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | YRI | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0324 | AFR | YRI | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0320 | AFR | ASW | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | ASW | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0072 | EUR | TSI | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0177 | EUR | TSI | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0279 | SAS | GIH | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA20905 | hp2 | a0001 | c0001 | t0006 | g0165 | SAS | GIH | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0203 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG01123 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0327 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02109 | hp2 | a0010 | c0012 | t0002 | g0030 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02486 | hp1 | a0001 | c0021 | t0004 | g0015 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0297 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ACB | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG03471 | hp2 | a0001 | c0001 | t0005 | g0152 | AFR | MSL | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG06807 | hp1 | a0001 | c0004 | t0002 | g0103 | AFR | USA | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | USA | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA18955 | hp2 | a0003 | c0005 | t0002 | g0060 | EAS | JPT | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | USA | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA20300 | hp2 | a0001 | c0004 | t0004 | g0005 | AFR | USA | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | LWK | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0064 | AFR | LWK | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0069 | REF | REF | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
homoSapiens | grch38p0 | a0001 | c0007 | t0002 | g0098 | REF | REF | GBF1_chr10_102240532_102387896 | GBF1 | chr10 | 102240532 | 102387896 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:102358061 | T | C | 1 | a0013 | 1 | HG03195.hp1 | missense_variant | MODERATE | c.662T>C | p.Met221Thr | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 9/40 | 922/6403 | 662/5583 | 221/1860 | chr10 | 102358061 | |||
chr10:102358118 | T | C | 1 | a0005 | 2 | HG00544.hp1 HG02135.hp2 |
missense_variant | MODERATE | c.719T>C | p.Met240Thr | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 9/40 | 979/6403 | 719/5583 | 240/1860 | chr10 | 102358118 | |||
chr10:102359382 | T | C | 1 | a0003 | 5 | HG02071.hp1 NA18952.hp1 NA18955.hp2 others(2): Show |
missense_variant | MODERATE | c.1127T>C | p.Met376Thr | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 11/40 | 1387/6403 | 1127/5583 | 376/1860 | chr10 | 102359382 | |||
chr10:102361741 | G | C | 1 | a0007 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.1515G>C | p.Glu505Asp | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/40 | 1775/6403 | 1515/5583 | 505/1860 | chr10 | 102361741 | |||
chr10:102366499 | G | A | 1 | a0011 | 1 | HG02818.hp2 | missense_variant | MODERATE | c.2426G>A | p.Arg809His | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 19/40 | 2686/6403 | 2426/5583 | 809/1860 | chr10 | 102366499 | |||
chr10:102370789 | G | A | 1 | a0010 | 1 | HG02109.hp2 | missense_variant | MODERATE | c.3589G>A | p.Val1197Met | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/40 | 3849/6403 | 3589/5583 | 1197/1860 | chr10 | 102370789 | |||
chr10:102370816 | C | T | 1 | a0004 | 3 | NA18949.hp2 NA18957.hp2 NA18994.hp2 |
missense_variant | MODERATE | c.3616C>T | p.Arg1206Cys | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/40 | 3876/6403 | 3616/5583 | 1206/1860 | chr10 | 102370816 | |||
chr10:102376430 | G | A | 1 | a0006 | 1 | HG00738.hp1 | missense_variant&splice_region_variant | MODERATE | c.4045G>A | p.Val1349Met | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 31/40 | 4305/6403 | 4045/5583 | 1349/1860 | chr10 | 102376430 | |||
chr10:102379548 | G | A | 1 | a0012 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.4673G>A | p.Arg1558Gln | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 35/40 | 4933/6403 | 4673/5583 | 1558/1860 | chr10 | 102379548 | |||
chr10:102380593 | G | A | 2 | a0002 a0008 |
13 | HG00735.hp2 HG01099.hp1 HG01123.hp1 others(10): Show |
missense_variant | MODERATE | c.5080G>A | p.Gly1694Ser | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 38/40 | 5340/6403 | 5080/5583 | 1694/1860 | chr10 | 102380593 | |||
chr10:102381186 | G | A | 1 | a0009 | 1 | HG01928.hp2 | missense_variant | MODERATE | c.5233G>A | p.Ala1745Thr | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/40 | 5493/6403 | 5233/5583 | 1745/1860 | chr10 | 102381186 | |||
chr10:102382195 | G | T | 1 | a0008 | 1 | HG01175.hp1 | missense_variant | MODERATE | c.5442G>T | p.Leu1814Phe | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 40/40 | 5702/6403 | 5442/5583 | 1814/1860 | chr10 | 102382195 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:102351860 | G | T | 1 | a0001c0024 | 1 | HG01081.hp1 | synonymous_variant | LOW | c.432G>T | p.Leu144Leu | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 6/40 | 692/6403 | 432/5583 | 144/1860 | chr10 | 102351860 | |||
chr10:102358516 | C | T | 1 | a0001c0023 | 1 | HG01106.hp1 | synonymous_variant | LOW | c.798C>T | p.Pro266Pro | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 10/40 | 1058/6403 | 798/5583 | 266/1860 | chr10 | 102358516 | |||
chr10:102358666 | G | A | 1 | a0011c0010 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.948G>A | p.Gly316Gly | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 10/40 | 1208/6403 | 948/5583 | 316/1860 | chr10 | 102358666 | |||
chr10:102363759 | A | G | 1 | a0011c0010 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.2067A>G | p.Pro689Pro | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/40 | 2327/6403 | 2067/5583 | 689/1860 | chr10 | 102363759 | |||
chr10:102365489 | C | T | 1 | a0001c0022 | 1 | NA19007.hp1 | synonymous_variant | LOW | c.2199C>T | p.Asp733Asp | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/40 | 2459/6403 | 2199/5583 | 733/1860 | chr10 | 102365489 | |||
chr10:102367555 | C | T | 1 | a0001c0021 | 1 | HG02486.hp1 | synonymous_variant | LOW | c.2637C>T | p.Ala879Ala | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 21/40 | 2897/6403 | 2637/5583 | 879/1860 | chr10 | 102367555 | |||
chr10:102376375 | G | A | 1 | a0001c0013 | 1 | HG01192.hp1 | synonymous_variant | LOW | c.3990G>A | p.Pro1330Pro | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 31/40 | 4250/6403 | 3990/5583 | 1330/1860 | chr10 | 102376375 | |||
chr10:102376405 | C | A | 1 | a0001c0014 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.4020C>A | p.Ala1340Ala | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 31/40 | 4280/6403 | 4020/5583 | 1340/1860 | chr10 | 102376405 | |||
chr10:102376586 | C | A | 1 | a0001c0016 | 1 | NA18994.hp1 | synonymous_variant | LOW | c.4074C>A | p.Ser1358Ser | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 32/40 | 4334/6403 | 4074/5583 | 1358/1860 | chr10 | 102376586 | |||
chr10:102376712 | T | C | 23 | a0001c0001 a0001c0003 a0001c0004 others(20): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
synonymous_variant | LOW | c.4200T>C | p.Ile1400Ile | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 32/40 | 4460/6403 | 4200/5583 | 1400/1860 | chr10 | 102376712 | |||
chr10:102376972 | A | G | 2 | a0001c0004 a0001c0021 |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
synonymous_variant | LOW | c.4326A>G | p.Lys1442Lys | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/40 | 4586/6403 | 4326/5583 | 1442/1860 | chr10 | 102376972 | |||
chr10:102377116 | G | A | 2 | a0001c0004 a0001c0021 |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
synonymous_variant | LOW | c.4470G>A | p.Thr1490Thr | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/40 | 4730/6403 | 4470/5583 | 1490/1860 | chr10 | 102377116 | |||
chr10:102380598 | C | T | 2 | a0001c0003 a0001c0024 |
12 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(9): Show |
synonymous_variant | LOW | c.5085C>T | p.Pro1695Pro | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 38/40 | 5345/6403 | 5085/5583 | 1695/1860 | chr10 | 102380598 | |||
chr10:102382294 | A | C | 1 | a0004c0020 | 1 | NA18994.hp2 | synonymous_variant | LOW | c.5541A>C | p.Thr1847Thr | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 40/40 | 5801/6403 | 5541/5583 | 1847/1860 | chr10 | 102382294 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:102245629 | G | A | 21 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(18): Show |
233 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(230): Show |
5_prime_UTR_variant | MODIFIER | c.-163G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/40 | 13310 | chr10 | 102245629 | ||||||
chr10:102245653 | T | C | 4 | a0001c0001t0003 a0001c0022t0003 a0001c0023t0003 others(1): Show |
68 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(65): Show |
5_prime_UTR_variant | MODIFIER | c.-139T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/40 | 13286 | chr10 | 102245653 | ||||||
chr10:102382536 | C | T | 1 | a0001c0001t0007 | 1 | NA18951.hp2 | 3_prime_UTR_variant | MODIFIER | c.*200C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 40/40 | 200 | chr10 | 102382536 | ||||||
chr10:102382537 | G | A | 1 | a0001c0001t0005 | 2 | HG00280.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*201G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 40/40 | 201 | chr10 | 102382537 | ||||||
chr10:102382632 | G | A | 1 | a0001c0001t0006 | 2 | HG03927.hp2 NA20905.hp2 |
3_prime_UTR_variant | MODIFIER | c.*296G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 40/40 | 296 | chr10 | 102382632 | ||||||
chr10:102382810 | G | A | 2 | a0001c0004t0004 a0001c0021t0004 |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*474G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 40/40 | 474 | chr10 | 102382810 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:102246022 | C | T | 6 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.-11+241C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102246022 | |||||||
chr10:102246258 | T | C | 1 | a0001c0001t0002g0003 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-11+477T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102246258 | |||||||
chr10:102246321 | G | T | 1 | a0001c0003t0001g0322 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-11+540G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102246321 | |||||||
chr10:102246331 | G | A | 1 | a0001c0001t0002g0004 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-11+550G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102246331 | |||||||
chr10:102246410 | T | C | 1 | a0001c0004t0004g0005 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-11+629T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102246410 | |||||||
chr10:102246527 | C | T | 1 | a0001c0001t0001g0321 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-11+746C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102246527 | |||||||
chr10:102246590 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-11+809T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102246590 | |||||||
chr10:102246817 | A | G | 1 | a0001c0001t0001g0320 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-11+1036A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102246817 | |||||||
chr10:102247028 | T | C | 1 | a0001c0001t0003g0007 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-11+1247T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102247028 | |||||||
chr10:102247049 | T | G | 1 | a0001c0001t0001g0008 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-11+1268T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102247049 | |||||||
chr10:102247097 | G | C | 2 | a0001c0001t0001g0009 a0001c0001t0001g0010 |
2 | HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.-11+1316G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102247097 | |||||||
chr10:102247275 | T | C | 1 | a0001c0001t0001g0011 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-11+1494T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102247275 | |||||||
chr10:102247286 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-11+1505G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102247286 | |||||||
chr10:102247526 | C | T | 1 | a0001c0001t0001g0319 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-11+1745C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102247526 | |||||||
chr10:102247735 | T | C | 1 | a0001c0001t0002g0013 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-11+1954T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102247735 | |||||||
chr10:102248278 | C | CT | 17 | a0001c0001t0003g0302 a0001c0001t0003g0303 a0001c0001t0003g0304 others(14): Show |
17 | HG00673.hp2 HG02071.hp2 HG02074.hp1 others(14): Show |
intron_variant | MODIFIER | c.-11+2509dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102248278 | ||||||
chr10:102248307 | C | T | 2 | a0001c0001t0001g0300 a0001c0001t0001g0301 |
2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.-11+2526C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248307 | |||||||
chr10:102248448 | T | C | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+2667T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248448 | |||||||
chr10:102248506 | C | T | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-11+2725C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248506 | |||||||
chr10:102248507 | G | T | 1 | a0001c0001t0002g0299 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-11+2726G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248507 | |||||||
chr10:102248523 | A | C | 232 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(229): Show |
233 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.-11+2742A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248523 | |||||||
chr10:102248771 | A | C | 2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-11+2990A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248771 | |||||||
chr10:102248870 | A | C | 1 | a0001c0007t0001g0328 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-11+3089A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248870 | |||||||
chr10:102248931 | A | C | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-11+3150A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248931 | |||||||
chr10:102248957 | A | C | 1 | a0001c0001t0002g0102 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-11+3176A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248957 | |||||||
chr10:102248964 | C | T | 1 | a0001c0001t0001g0296 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-11+3183C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248964 | |||||||
chr10:102248994 | G | A | 238 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(235): Show |
240 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.-11+3213G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102248994 | |||||||
chr10:102249113 | G | C | 238 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(235): Show |
240 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.-11+3332G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102249113 | |||||||
chr10:102249423 | G | T | 1 | a0001c0001t0001g0295 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-11+3642G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102249423 | |||||||
chr10:102249437 | A | C | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-11+3656A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102249437 | |||||||
chr10:102249746 | C | A | 57 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0017 others(54): Show |
57 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.-11+3965C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102249746 | |||||||
chr10:102249932 | C | T | 2 | a0001c0001t0001g0293 a0001c0001t0001g0319 |
2 | NA18963.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.-11+4151C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102249932 | |||||||
chr10:102250092 | GT | G | 232 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(229): Show |
233 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(230): Show |
intron_variant | MODIFIER | c.-11+4316delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102250092 | ||||||
chr10:102250106 | G | T | 1 | a0001c0001t0001g0292 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-11+4325G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102250106 | |||||||
chr10:102250176 | A | G | 1 | a0001c0001t0003g0291 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-11+4395A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102250176 | |||||||
chr10:102250385 | A | G | 86 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0230 others(83): Show |
87 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.-11+4604A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102250385 | |||||||
chr10:102250524 | AT | A | 16 | a0001c0001t0001g0229 a0001c0001t0001g0323 a0001c0001t0001g0324 others(13): Show |
17 | HG01069.hp2 HG01891.hp1 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.-11+4762delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102250524 | ||||||
chr10:102250524 | ATT | A | 218 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(215): Show |
219 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(216): Show |
intron_variant | MODIFIER | c.-11+4761_-11+4762d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102250524 | ||||||
chr10:102250524 | ATTT | A | 7 | a0001c0001t0001g0011 a0001c0001t0001g0105 a0001c0001t0001g0106 others(4): Show |
7 | HG01516.hp1 HG01516.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.-11+4760_-11+4762d others(5): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102250524 | ||||||
chr10:102250880 | C | G | 3 | a0001c0001t0002g0013 a0001c0001t0002g0070 a0001c0001t0002g0071 |
3 | HG01346.hp1 HG01361.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-11+5099C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102250880 | |||||||
chr10:102250926 | C | T | 1 | a0001c0024t0001g0228 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-11+5145C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102250926 | |||||||
chr10:102250945 | G | A | 140 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(137): Show |
141 | HG00099.hp1 HG00544.hp2 HG00558.hp2 others(138): Show |
intron_variant | MODIFIER | c.-11+5164G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102250945 | |||||||
chr10:102251008 | GA | G | 7 | a0001c0001t0003g0235 a0001c0004t0002g0103 a0001c0004t0004g0001 others(4): Show |
8 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-11+5240delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102251008 | ||||||
chr10:102251008 | GAA | G | 227 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(224): Show |
228 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(225): Show |
intron_variant | MODIFIER | c.-11+5239_-11+5240d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102251008 | ||||||
chr10:102251214 | G | C | 86 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0230 others(83): Show |
87 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.-11+5433G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102251214 | |||||||
chr10:102251343 | G | T | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-11+5562G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102251343 | |||||||
chr10:102251560 | A | G | 25 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0212 others(22): Show |
25 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.-11+5779A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102251560 | |||||||
chr10:102251573 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0151 |
2 | HG00738.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.-11+5792A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102251573 | |||||||
chr10:102251643 | T | G | 1 | a0001c0001t0001g0236 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-11+5862T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102251643 | |||||||
chr10:102251703 | G | A | 1 | a0001c0001t0001g0012 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-11+5922G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102251703 | |||||||
chr10:102251723 | T | A | 3 | a0001c0001t0003g0237 a0001c0001t0003g0238 a0001c0001t0003g0239 |
3 | HG01943.hp1 HG02004.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.-11+5942T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102251723 | |||||||
chr10:102251750 | C | G | 1 | a0001c0001t0002g0068 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-11+5969C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102251750 | |||||||
chr10:102251922 | C | A | 1 | a0001c0003t0001g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-11+6141C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102251922 | |||||||
chr10:102251940 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-11+6159C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102251940 | |||||||
chr10:102251963 | TCAGGAGT others(7): Show |
T | 1 | a0001c0001t0005g0152 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-11+6200_-11+6213d others(16): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102251963 | ||||||
chr10:102252196 | C | T | 24 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0001g0213 others(21): Show |
24 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-11+6415C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252196 | |||||||
chr10:102252208 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-11+6427G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252208 | |||||||
chr10:102252331 | G | A | 3 | a0001c0001t0001g0154 a0001c0001t0003g0302 a0001c0001t0003g0303 |
3 | HG02071.hp2 HG02074.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-11+6550G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252331 | |||||||
chr10:102252378 | A | G | 1 | a0001c0001t0002g0067 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-10-6551A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252378 | |||||||
chr10:102252485 | A | G | 1 | a0003c0005t0002g0101 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-10-6444A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252485 | |||||||
chr10:102252528 | G | A | 7 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(4): Show |
7 | HG01106.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-6401G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252528 | |||||||
chr10:102252568 | G | A | 1 | a0001c0001t0003g0235 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.-10-6361G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252568 | |||||||
chr10:102252671 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-10-6258G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252671 | |||||||
chr10:102252825 | C | T | 3 | a0001c0003t0001g0226 a0001c0003t0001g0227 a0001c0024t0001g0228 |
3 | HG01081.hp1 HG02451.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-10-6104C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252825 | |||||||
chr10:102252920 | T | C | 238 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(235): Show |
240 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.-10-6009T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252920 | |||||||
chr10:102252921 | G | A | 2 | a0001c0001t0001g0240 a0007c0011t0001g0294 |
2 | HG01074.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.-10-6008G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102252921 | |||||||
chr10:102253040 | C | A | 1 | a0001c0001t0003g0241 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-10-5889C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253040 | |||||||
chr10:102253041 | C | T | 1 | a0001c0001t0003g0241 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-10-5888C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253041 | |||||||
chr10:102253042 | C | G | 1 | a0001c0001t0003g0241 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-10-5887C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253042 | |||||||
chr10:102253043 | T | A | 1 | a0001c0001t0003g0241 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-10-5886T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253043 | |||||||
chr10:102253045 | C | T | 1 | a0001c0001t0003g0241 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-10-5884C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253045 | |||||||
chr10:102253046 | C | A | 1 | a0001c0001t0003g0241 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-10-5883C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253046 | |||||||
chr10:102253184 | T | C | 238 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(235): Show |
240 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.-10-5745T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253184 | |||||||
chr10:102253335 | G | C | 238 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(235): Show |
240 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.-10-5594G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253335 | |||||||
chr10:102253577 | G | T | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-5352G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253577 | |||||||
chr10:102253765 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-10-5164C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253765 | |||||||
chr10:102253783 | G | C | 7 | a0001c0001t0002g0073 a0001c0001t0002g0074 a0001c0001t0002g0075 others(4): Show |
7 | HG02071.hp1 HG02135.hp1 NA18952.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-5146G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253783 | |||||||
chr10:102253838 | C | G | 5 | a0002c0002t0001g0107 a0002c0002t0001g0202 a0002c0002t0001g0203 others(2): Show |
5 | HG00735.hp2 HG01123.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-5091C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253838 | |||||||
chr10:102253947 | C | T | 3 | a0001c0001t0002g0018 a0001c0001t0002g0065 a0001c0001t0002g0066 |
3 | HG01069.hp2 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.-10-4982C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102253947 | |||||||
chr10:102254134 | A | G | 1 | a0001c0001t0001g0150 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-10-4795A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102254134 | |||||||
chr10:102254198 | T | C | 3 | a0001c0001t0001g0114 a0001c0001t0005g0152 a0001c0001t0005g0155 |
3 | HG00280.hp1 HG03471.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-10-4731T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102254198 | |||||||
chr10:102254463 | G | C | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-4466G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102254463 | |||||||
chr10:102254483 | T | C | 1 | a0001c0001t0002g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-10-4446T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102254483 | |||||||
chr10:102254666 | G | A | 1 | a0001c0001t0003g0002 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-10-4263G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102254666 | |||||||
chr10:102254775 | T | TATTTCTC others(461): Show |
2 | a0001c0001t0003g0231 a0001c0001t0003g0232 |
2 | NA18959.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.-10-4138_-10-4137i others(470): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102254775 | ||||||
chr10:102254775 | T | TATTTCTC others(462): Show |
2 | a0001c0001t0003g0233 a0001c0022t0003g0234 |
2 | HG00609.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-10-4138_-10-4137i others(471): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102254775 | ||||||
chr10:102255056 | T | C | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-3873T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102255056 | |||||||
chr10:102255101 | C | T | 1 | a0001c0001t0002g0064 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-10-3828C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102255101 | |||||||
chr10:102255114 | C | T | 1 | a0001c0001t0001g0301 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-10-3815C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102255114 | |||||||
chr10:102255150 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-10-3779C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102255150 | |||||||
chr10:102255241 | A | G | 1 | a0001c0001t0002g0100 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-10-3688A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102255241 | |||||||
chr10:102255497 | A | G | 5 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-3432A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102255497 | |||||||
chr10:102255522 | A | G | 78 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0230 others(75): Show |
79 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.-10-3407A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102255522 | |||||||
chr10:102255955 | TATTATTT others(4): Show |
T | 1 | a0001c0001t0003g0250 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-10-2972_-10-2962d others(13): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102255955 | ||||||
chr10:102255967 | A | G | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-10-2962A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102255967 | |||||||
chr10:102255980 | C | T | 7 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(4): Show |
7 | HG01106.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-10-2949C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102255980 | |||||||
chr10:102256061 | G | T | 238 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(235): Show |
240 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(237): Show |
intron_variant | MODIFIER | c.-10-2868G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102256061 | |||||||
chr10:102256076 | A | G | 1 | a0002c0002t0001g0205 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-10-2853A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102256076 | |||||||
chr10:102256165 | G | A | 1 | a0001c0003t0001g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-10-2764G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102256165 | |||||||
chr10:102256423 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-10-2506T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102256423 | |||||||
chr10:102256508 | T | TA | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-2409dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102256508 | ||||||
chr10:102256558 | C | G | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-2371C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102256558 | |||||||
chr10:102256562 | CTGGA | C | 324 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(321): Show |
326 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.-10-2362_-10-2359d others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102256562 | ||||||
chr10:102256773 | A | T | 1 | a0001c0001t0002g0097 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-10-2156A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102256773 | |||||||
chr10:102256834 | T | C | 2 | a0005c0006t0001g0156 a0005c0006t0001g0157 |
2 | HG00544.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.-10-2095T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102256834 | |||||||
chr10:102257121 | G | A | 5 | a0001c0001t0001g0230 a0001c0001t0001g0251 a0001c0001t0001g0252 others(2): Show |
5 | HG02922.hp1 HG03041.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-10-1808G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102257121 | |||||||
chr10:102257289 | T | G | 4 | a0001c0001t0001g0230 a0001c0001t0001g0251 a0001c0001t0001g0252 others(1): Show |
4 | HG02922.hp1 HG03041.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-10-1640T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102257289 | |||||||
chr10:102257365 | G | A | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-10-1564G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102257365 | |||||||
chr10:102257384 | C | G | 1 | a0001c0001t0002g0299 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-10-1545C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102257384 | |||||||
chr10:102257421 | G | A | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-1508G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102257421 | |||||||
chr10:102257616 | G | C | 1 | a0001c0001t0005g0152 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-10-1313G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102257616 | |||||||
chr10:102257864 | G | C | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-1065G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102257864 | |||||||
chr10:102257877 | G | C | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-10-1052G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102257877 | |||||||
chr10:102257988 | G | A | 5 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-941G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102257988 | |||||||
chr10:102258150 | A | AT | 6 | a0001c0001t0002g0013 a0001c0001t0002g0019 a0001c0001t0002g0062 others(3): Show |
6 | HG00280.hp2 HG00738.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.-10-757dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102258150 | ||||||
chr10:102258150 | AT | A | 128 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0011 others(125): Show |
128 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.-10-757delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102258150 | ||||||
chr10:102258150 | ATT | A | 93 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0109 others(90): Show |
94 | HG00609.hp1 HG00673.hp2 HG00735.hp1 others(91): Show |
intron_variant | MODIFIER | c.-10-758_-10-757del others(2): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102258150 | ||||||
chr10:102258150 | ATTT | A | 15 | a0001c0001t0001g0117 a0001c0001t0001g0296 a0001c0001t0003g0237 others(12): Show |
16 | HG00642.hp2 HG01943.hp1 HG02004.hp1 others(13): Show |
intron_variant | MODIFIER | c.-10-759_-10-757del others(3): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102258150 | ||||||
chr10:102258228 | T | C | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-10-701T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102258228 | |||||||
chr10:102258275 | C | T | 5 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.-10-654C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102258275 | |||||||
chr10:102258384 | G | A | 1 | a0001c0001t0003g0260 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-10-545G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102258384 | |||||||
chr10:102258774 | C | CAA | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.-10-136_-10-135dup others(2): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102258774 | ||||||
chr10:102258774 | CA | C | 19 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0196 others(16): Show |
19 | HG01074.hp1 HG01258.hp1 HG01516.hp2 others(16): Show |
intron_variant | MODIFIER | c.-10-135delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102258774 | ||||||
chr10:102258774 | CAAAAAAA others(5): Show |
C | 86 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0230 others(83): Show |
87 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(84): Show |
intron_variant | MODIFIER | c.-10-146_-10-135del others(12): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | INFO_REALIGN_3_PRIME | chr10 | 102258774 | ||||||
chr10:102258889 | C | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG00544.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.-10-40C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 1/39 | chr10 | 102258889 | |||||||
chr10:102259279 | T | G | 1 | a0001c0001t0002g0022 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.96+245T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 2/39 | chr10 | 102259279 | |||||||
chr10:102259452 | A | G | 1 | a0001c0001t0002g0067 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.96+418A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 2/39 | chr10 | 102259452 | |||||||
chr10:102259690 | C | A | 295 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(292): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.97-360C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 2/39 | chr10 | 102259690 | |||||||
chr10:102259732 | A | G | 9 | a0001c0001t0001g0240 a0001c0001t0001g0242 a0001c0001t0001g0243 others(6): Show |
9 | HG01169.hp1 HG01256.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.97-318A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 2/39 | chr10 | 102259732 | |||||||
chr10:102259767 | T | C | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.97-283T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 2/39 | chr10 | 102259767 | |||||||
chr10:102259999 | T | C | 3 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 |
4 | HG02280.hp1 NA18522.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.97-51T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 2/39 | chr10 | 102259999 | |||||||
chr10:102260473 | C | CTT | 11 | a0001c0001t0001g0011 a0001c0001t0001g0160 a0001c0001t0001g0212 others(8): Show |
11 | HG01070.hp2 HG01109.hp1 HG01516.hp2 others(8): Show |
intron_variant | MODIFIER | c.163+358_163+359dup others(2): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102260473 | ||||||
chr10:102260473 | C | CTTT | 163 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(160): Show |
163 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(160): Show |
intron_variant | MODIFIER | c.163+359_163+360ins others(3): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102260473 | ||||||
chr10:102260473 | C | CTTTT | 46 | a0001c0001t0001g0010 a0001c0001t0001g0113 a0001c0001t0001g0116 others(43): Show |
47 | HG00558.hp2 HG00735.hp2 HG01070.hp1 others(44): Show |
intron_variant | MODIFIER | c.163+359_163+360ins others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102260473 | ||||||
chr10:102260473 | C | CTTTTTTT others(2): Show |
5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG01074.hp1 HG02280.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+359_163+360ins others(9): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102260473 | ||||||
chr10:102260473 | C | CTTTTTTT others(3): Show |
6 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0292 others(3): Show |
6 | HG01106.hp2 HG02615.hp1 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+359_163+360ins others(10): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102260473 | ||||||
chr10:102260473 | C | CTTTTTTT others(4): Show |
2 | a0001c0001t0001g0111 a0011c0010t0001g0112 |
2 | HG02818.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.163+359_163+360ins others(11): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102260473 | ||||||
chr10:102260476 | C | CT | 11 | a0001c0001t0002g0058 a0001c0001t0002g0059 a0001c0001t0002g0090 others(8): Show |
11 | HG02027.hp1 HG02970.hp2 NA18953.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+383dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102260476 | ||||||
chr10:102260476 | C | T | 236 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(233): Show |
238 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(235): Show |
intron_variant | MODIFIER | c.163+360C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102260476 | |||||||
chr10:102260566 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163+450C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102260566 | |||||||
chr10:102260600 | C | T | 1 | a0002c0002t0001g0205 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.163+484C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102260600 | |||||||
chr10:102260635 | A | G | 2 | a0001c0003t0001g0206 a0001c0003t0001g0224 |
2 | HG02976.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.163+519A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102260635 | |||||||
chr10:102260743 | C | T | 1 | a0001c0001t0003g0002 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.163+627C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102260743 | |||||||
chr10:102261231 | A | T | 1 | a0001c0001t0001g0106 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.163+1115A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261231 | |||||||
chr10:102261235 | TTG | T | 267 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(264): Show |
269 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(266): Show |
intron_variant | MODIFIER | c.163+1141_163+1142d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102261235 | ||||||
chr10:102261235 | TTGTGTGT others(7): Show |
T | 27 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0207 others(24): Show |
27 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(24): Show |
intron_variant | MODIFIER | c.163+1129_163+1142d others(16): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102261235 | ||||||
chr10:102261277 | T | C | 18 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0117 others(15): Show |
18 | HG01109.hp2 HG01891.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.163+1161T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261277 | |||||||
chr10:102261277 | T | TAC | 3 | a0001c0001t0001g0207 a0001c0001t0002g0063 a0001c0001t0003g0241 |
3 | HG01099.hp2 HG04115.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.163+1177_163+1178d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102261277 | ||||||
chr10:102261328 | A | G | 59 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(56): Show |
59 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.163+1212A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261328 | |||||||
chr10:102261352 | G | C | 26 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0208 others(23): Show |
26 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(23): Show |
intron_variant | MODIFIER | c.163+1236G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261352 | |||||||
chr10:102261581 | C | CT | 4 | a0001c0001t0002g0086 a0001c0001t0002g0087 a0001c0001t0002g0088 others(1): Show |
4 | HG00558.hp1 HG00621.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+1466dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102261581 | ||||||
chr10:102261615 | C | CT | 14 | a0001c0001t0002g0021 a0001c0001t0002g0052 a0001c0001t0002g0053 others(11): Show |
15 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(12): Show |
intron_variant | MODIFIER | c.163+1517dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102261615 | ||||||
chr10:102261615 | CT | C | 223 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(220): Show |
224 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(221): Show |
intron_variant | MODIFIER | c.163+1517delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102261615 | ||||||
chr10:102261620 | T | C | 6 | a0001c0001t0001g0230 a0001c0001t0001g0236 a0001c0001t0001g0251 others(3): Show |
6 | HG02258.hp1 HG02922.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+1504T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261620 | |||||||
chr10:102261633 | T | G | 1 | a0001c0001t0003g0241 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.163+1517T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261633 | |||||||
chr10:102261748 | A | G | 1 | a0001c0001t0001g0150 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.163+1632A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261748 | |||||||
chr10:102261784 | A | G | 295 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(292): Show |
297 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(294): Show |
intron_variant | MODIFIER | c.163+1668A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261784 | |||||||
chr10:102261911 | C | T | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+1795C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261911 | |||||||
chr10:102261951 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.163+1835C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261951 | |||||||
chr10:102261955 | GCT | G | 7 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0092 others(4): Show |
7 | HG02027.hp1 NA18953.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+1841_163+1842d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102261955 | ||||||
chr10:102261960 | C | G | 7 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0092 others(4): Show |
7 | HG02027.hp1 NA18953.hp1 NA18967.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+1844C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102261960 | |||||||
chr10:102262000 | T | C | 2 | a0001c0001t0003g0231 a0001c0001t0003g0233 |
2 | HG00609.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.163+1884T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102262000 | |||||||
chr10:102262253 | C | A | 1 | a0001c0001t0003g0262 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.163+2137C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102262253 | |||||||
chr10:102262543 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0111 |
2 | HG01106.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.163+2427G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102262543 | |||||||
chr10:102262621 | C | T | 1 | a0001c0001t0002g0050 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.163+2505C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102262621 | |||||||
chr10:102262656 | T | C | 1 | a0001c0001t0002g0024 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.163+2540T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102262656 | |||||||
chr10:102262849 | C | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0111 |
2 | HG01106.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.163+2733C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102262849 | |||||||
chr10:102262956 | A | G | 1 | a0001c0001t0003g0314 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.163+2840A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102262956 | |||||||
chr10:102263054 | G | T | 1 | a0003c0005t0002g0060 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.163+2938G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102263054 | |||||||
chr10:102263208 | C | T | 3 | a0001c0001t0002g0003 a0001c0001t0002g0049 a0001c0001t0002g0089 |
3 | HG00621.hp2 HG00673.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.163+3092C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102263208 | |||||||
chr10:102263541 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.163+3425C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102263541 | |||||||
chr10:102263542 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.163+3426A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102263542 | |||||||
chr10:102264114 | C | T | 121 | a0001c0001t0001g0154 a0001c0001t0001g0207 a0001c0001t0001g0208 others(118): Show |
122 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.163+3998C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102264114 | |||||||
chr10:102264230 | C | T | 1 | a0012c0017t0001g0192 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.163+4114C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102264230 | |||||||
chr10:102264269 | G | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG01109.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.163+4153G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102264269 | |||||||
chr10:102265589 | G | A | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+5473G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102265589 | |||||||
chr10:102265626 | A | G | 94 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(91): Show |
95 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.163+5510A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102265626 | |||||||
chr10:102265653 | C | G | 56 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(53): Show |
56 | HG00544.hp1 HG00609.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.163+5537C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102265653 | |||||||
chr10:102265683 | C | CAATG | 3 | a0001c0001t0003g0261 a0001c0001t0003g0318 a0007c0011t0001g0294 |
3 | HG01074.hp1 NA18963.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.163+5594_163+5597d others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102265683 | ||||||
chr10:102266021 | A | G | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+5905A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102266021 | |||||||
chr10:102266050 | A | C | 1 | a0001c0001t0001g0130 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.163+5934A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102266050 | |||||||
chr10:102266112 | G | A | 1 | a0001c0001t0002g0059 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.163+5996G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102266112 | |||||||
chr10:102266195 | T | C | 320 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(317): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.163+6079T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102266195 | |||||||
chr10:102266217 | T | G | 1 | a0001c0001t0002g0089 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.163+6101T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102266217 | |||||||
chr10:102267418 | T | C | 4 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
4 | NA19002.hp1 NA19005.hp2 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+7302T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102267418 | |||||||
chr10:102267502 | T | TCAA | 89 | a0001c0001t0001g0253 a0001c0001t0002g0003 a0001c0001t0002g0004 others(86): Show |
89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.163+7411_163+7413d others(5): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102267502 | ||||||
chr10:102267546 | T | C | 1 | a0001c0001t0002g0081 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.163+7430T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102267546 | |||||||
chr10:102267737 | G | T | 1 | a0001c0001t0002g0056 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.163+7621G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102267737 | |||||||
chr10:102268294 | C | G | 325 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(322): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.163+8178C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102268294 | |||||||
chr10:102268365 | A | C | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+8249A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102268365 | |||||||
chr10:102268750 | C | A | 87 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(84): Show |
87 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.163+8634C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102268750 | |||||||
chr10:102268945 | T | C | 3 | a0001c0001t0006g0164 a0001c0001t0006g0165 a0012c0017t0001g0192 |
3 | HG03017.hp1 HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.163+8829T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102268945 | |||||||
chr10:102269180 | G | A | 1 | a0001c0014t0001g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.163+9064G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102269180 | |||||||
chr10:102269289 | G | A | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+9173G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102269289 | |||||||
chr10:102269371 | G | T | 1 | a0001c0001t0001g0254 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.163+9255G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102269371 | |||||||
chr10:102269428 | C | G | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+9312C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102269428 | |||||||
chr10:102269550 | A | C | 16 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0131 others(13): Show |
16 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.163+9434A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102269550 | |||||||
chr10:102269709 | C | T | 5 | a0001c0003t0001g0108 a0001c0003t0001g0209 a0001c0003t0001g0210 others(2): Show |
5 | HG01070.hp2 HG01516.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+9593C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102269709 | |||||||
chr10:102269880 | A | AT | 6 | a0001c0001t0001g0191 a0001c0001t0002g0024 a0001c0001t0002g0047 others(3): Show |
6 | HG01123.hp2 HG01175.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+9780dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102269880 | ||||||
chr10:102269965 | G | A | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+9849G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102269965 | |||||||
chr10:102270035 | T | C | 89 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(86): Show |
89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.163+9919T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102270035 | |||||||
chr10:102270046 | T | C | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.163+9930T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102270046 | |||||||
chr10:102270253 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.163+10137T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102270253 | |||||||
chr10:102270361 | G | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0151 |
2 | HG00738.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.163+10245G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102270361 | |||||||
chr10:102270437 | T | C | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+10321T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102270437 | |||||||
chr10:102270444 | G | A | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.163+10328G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102270444 | |||||||
chr10:102270845 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.163+10729T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102270845 | |||||||
chr10:102270857 | C | T | 1 | a0001c0001t0005g0152 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.163+10741C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102270857 | |||||||
chr10:102271035 | T | C | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10919T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271035 | |||||||
chr10:102271036 | T | C | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10920T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271036 | |||||||
chr10:102271038 | T | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10922T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271038 | |||||||
chr10:102271039 | T | G | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10923T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271039 | |||||||
chr10:102271040 | A | G | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10924A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271040 | |||||||
chr10:102271041 | T | G | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10925T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271041 | |||||||
chr10:102271042 | T | G | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10926T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271042 | |||||||
chr10:102271044 | T | C | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10928T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271044 | |||||||
chr10:102271046 | A | G | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10930A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271046 | |||||||
chr10:102271047 | T | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10931T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271047 | |||||||
chr10:102271050 | T | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10934T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271050 | |||||||
chr10:102271052 | T | G | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10936T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271052 | |||||||
chr10:102271053 | T | G | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10937T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271053 | |||||||
chr10:102271059 | A | C | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10943A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271059 | |||||||
chr10:102271065 | T | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10949T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271065 | |||||||
chr10:102271067 | T | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10951T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271067 | |||||||
chr10:102271068 | T | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10952T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271068 | |||||||
chr10:102271070 | C | G | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10954C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271070 | |||||||
chr10:102271071 | T | C | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10955T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271071 | |||||||
chr10:102271077 | G | C | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10961G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271077 | |||||||
chr10:102271079 | C | T | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10963C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271079 | |||||||
chr10:102271080 | C | G | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10964C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271080 | |||||||
chr10:102271082 | G | T | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10966G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271082 | |||||||
chr10:102271084 | C | G | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10968C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271084 | |||||||
chr10:102271088 | A | C | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10972A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271088 | |||||||
chr10:102271092 | C | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10976C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271092 | |||||||
chr10:102271099 | G | C | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10983G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271099 | |||||||
chr10:102271104 | C | T | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10988C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271104 | |||||||
chr10:102271111 | C | T | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10995C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271111 | |||||||
chr10:102271113 | C | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+10997C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271113 | |||||||
chr10:102271118 | A | T | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11002A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271118 | |||||||
chr10:102271119 | G | C | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11003G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271119 | |||||||
chr10:102271121 | T | C | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11005T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271121 | |||||||
chr10:102271123 | C | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11007C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271123 | |||||||
chr10:102271126 | C | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11010C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271126 | |||||||
chr10:102271127 | T | C | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11011T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271127 | |||||||
chr10:102271128 | C | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11012C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271128 | |||||||
chr10:102271130 | T | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11014T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271130 | |||||||
chr10:102271130 | T | C | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+11014T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271130 | |||||||
chr10:102271131 | G | A | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+11015G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271131 | |||||||
chr10:102271132 | G | C | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11016G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271132 | |||||||
chr10:102271133 | G | C | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11017G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271133 | |||||||
chr10:102271138 | T | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11022T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271138 | |||||||
chr10:102271140 | C | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11024C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271140 | |||||||
chr10:102271141 | C | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11025C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271141 | |||||||
chr10:102271142 | A | C | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11026A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271142 | |||||||
chr10:102271144 | T | G | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11028T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271144 | |||||||
chr10:102271145 | C | G | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11029C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271145 | |||||||
chr10:102271146 | T | C | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11030T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271146 | |||||||
chr10:102271149 | T | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11033T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271149 | |||||||
chr10:102271150 | G | C | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11034G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271150 | |||||||
chr10:102271151 | C | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11035C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271151 | |||||||
chr10:102271152 | C | G | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11036C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271152 | |||||||
chr10:102271157 | C | T | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11041C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271157 | |||||||
chr10:102271161 | C | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11045C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271161 | |||||||
chr10:102271164 | A | T | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11048A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271164 | |||||||
chr10:102271165 | G | T | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11049G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271165 | |||||||
chr10:102271167 | A | G | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11051A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271167 | |||||||
chr10:102271171 | G | T | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11055G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271171 | |||||||
chr10:102271173 | G | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11057G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271173 | |||||||
chr10:102271175 | C | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11059C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271175 | |||||||
chr10:102271183 | G | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11067G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271183 | |||||||
chr10:102271186 | C | T | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11070C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271186 | |||||||
chr10:102271187 | G | A | 1 | a0002c0002t0001g0104 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.163+11071G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271187 | |||||||
chr10:102271189 | C | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11073C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271189 | |||||||
chr10:102271194 | C | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11078C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271194 | |||||||
chr10:102271195 | G | T | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11079G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271195 | |||||||
chr10:102271196 | C | CAAAGATC others(6): Show |
1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11080_163+1108 others(17): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271196 | |||||||
chr10:102271197 | C | G | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11081C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271197 | |||||||
chr10:102271199 | G | A | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11083G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271199 | |||||||
chr10:102271200 | G | T | 1 | a0001c0001t0002g0090 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.163+11084G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271200 | |||||||
chr10:102271293 | T | C | 5 | a0001c0001t0001g0159 a0001c0001t0001g0168 a0001c0001t0001g0169 others(2): Show |
5 | NA18971.hp2 NA18982.hp1 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+11177T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271293 | |||||||
chr10:102271317 | G | A | 1 | a0001c0001t0003g0255 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.163+11201G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271317 | |||||||
chr10:102271461 | A | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG01109.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.163+11345A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271461 | |||||||
chr10:102271514 | C | CT | 87 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0190 others(84): Show |
88 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.163+11413dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102271514 | ||||||
chr10:102271514 | CT | C | 11 | a0001c0001t0001g0011 a0001c0001t0001g0113 a0001c0001t0001g0133 others(8): Show |
11 | HG01358.hp2 HG01496.hp2 HG02135.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+11413delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102271514 | ||||||
chr10:102271532 | T | C | 94 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(91): Show |
95 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.163+11416T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271532 | |||||||
chr10:102271604 | C | T | 2 | a0001c0001t0002g0046 a0001c0001t0002g0067 |
2 | HG03492.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.163+11488C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271604 | |||||||
chr10:102271641 | G | A | 320 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(317): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.163+11525G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271641 | |||||||
chr10:102271704 | T | G | 1 | a0001c0001t0003g0306 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.163+11588T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102271704 | |||||||
chr10:102272023 | G | T | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+11907G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102272023 | |||||||
chr10:102272112 | A | AT | 140 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0109 others(137): Show |
141 | HG00099.hp1 HG00558.hp1 HG00609.hp1 others(138): Show |
intron_variant | MODIFIER | c.163+12009dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102272112 | ||||||
chr10:102272112 | AT | A | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+12009delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102272112 | ||||||
chr10:102272219 | C | T | 2 | a0001c0001t0001g0212 a0001c0001t0001g0213 |
2 | HG01109.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.163+12103C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102272219 | |||||||
chr10:102272455 | A | C | 1 | a0001c0001t0002g0051 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.163+12339A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102272455 | |||||||
chr10:102272526 | G | A | 1 | a0001c0001t0002g0086 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.163+12410G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102272526 | |||||||
chr10:102273546 | T | G | 3 | a0001c0001t0002g0023 a0001c0001t0002g0025 a0001c0001t0002g0047 |
3 | NA18944.hp2 NA18979.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.163+13430T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102273546 | |||||||
chr10:102273658 | C | T | 3 | a0001c0001t0003g0284 a0001c0001t0003g0285 a0001c0001t0003g0286 |
3 | NA18979.hp1 NA19002.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.163+13542C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102273658 | |||||||
chr10:102274218 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.163+14102G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102274218 | |||||||
chr10:102274330 | T | C | 94 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(91): Show |
95 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.163+14214T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102274330 | |||||||
chr10:102274556 | A | G | 1 | a0001c0001t0003g0276 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.163+14440A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102274556 | |||||||
chr10:102274699 | A | AT | 11 | a0001c0001t0001g0006 a0001c0001t0001g0113 a0001c0001t0001g0133 others(8): Show |
11 | HG00558.hp2 HG01175.hp2 HG01192.hp2 others(8): Show |
intron_variant | MODIFIER | c.163+14613dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102274699 | ||||||
chr10:102274699 | A | ATT | 24 | a0001c0001t0001g0140 a0001c0001t0001g0208 a0001c0001t0001g0212 others(21): Show |
24 | HG00673.hp1 HG01070.hp2 HG01081.hp1 others(21): Show |
intron_variant | MODIFIER | c.163+14612_163+1461 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102274699 | ||||||
chr10:102274699 | A | ATTT | 31 | a0001c0001t0001g0213 a0001c0001t0001g0219 a0001c0001t0001g0223 others(28): Show |
31 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(28): Show |
intron_variant | MODIFIER | c.163+14611_163+1461 others(7): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102274699 | ||||||
chr10:102274699 | A | ATTTT | 19 | a0001c0001t0001g0220 a0001c0001t0002g0013 a0001c0001t0002g0019 others(16): Show |
19 | HG01123.hp2 HG01346.hp1 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.163+14610_163+1461 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102274699 | ||||||
chr10:102274699 | AT | A | 79 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0115 others(76): Show |
79 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(76): Show |
intron_variant | MODIFIER | c.163+14613delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102274699 | ||||||
chr10:102274699 | ATT | A | 66 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0109 others(63): Show |
67 | HG00099.hp1 HG00673.hp2 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.163+14612_163+1461 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102274699 | ||||||
chr10:102274699 | ATTTTTTT others(3): Show |
A | 25 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0074 others(22): Show |
25 | HG00558.hp1 HG00621.hp2 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.163+14604_163+1461 others(14): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102274699 | ||||||
chr10:102274699 | ATTTTTTT others(4): Show |
A | 3 | a0001c0001t0002g0004 a0001c0001t0002g0091 a0001c0001t0002g0092 |
3 | HG01069.hp1 NA18967.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.163+14603_163+1461 others(15): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102274699 | ||||||
chr10:102274699 | ATTTTTTT others(5): Show |
A | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+14602_163+1461 others(16): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102274699 | ||||||
chr10:102274701 | T | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG00544.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.163+14585T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102274701 | |||||||
chr10:102274793 | C | T | 21 | a0001c0001t0001g0011 a0001c0001t0001g0113 a0001c0001t0001g0133 others(18): Show |
21 | HG01169.hp1 HG01256.hp1 HG01258.hp2 others(18): Show |
intron_variant | MODIFIER | c.163+14677C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102274793 | |||||||
chr10:102274877 | A | G | 1 | a0001c0001t0002g0072 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.163+14761A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102274877 | |||||||
chr10:102275011 | C | CT | 16 | a0001c0001t0001g0124 a0001c0001t0001g0140 a0001c0001t0001g0323 others(13): Show |
17 | HG00741.hp1 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.163+14913dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102275011 | ||||||
chr10:102275011 | CT | C | 84 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(81): Show |
84 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.163+14913delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102275011 | ||||||
chr10:102275023 | T | C | 59 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(56): Show |
59 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.163+14907T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102275023 | |||||||
chr10:102275901 | G | C | 3 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0038 |
3 | HG02523.hp2 NA19004.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.163+15785G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102275901 | |||||||
chr10:102276251 | G | A | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.163+16135G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102276251 | |||||||
chr10:102276254 | C | T | 3 | a0001c0001t0001g0230 a0001c0001t0001g0251 a0001c0001t0001g0252 |
3 | HG03041.hp2 HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.163+16138C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102276254 | |||||||
chr10:102276394 | C | T | 2 | a0001c0001t0003g0313 a0001c0001t0003g0316 |
2 | HG02148.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.163+16278C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102276394 | |||||||
chr10:102276525 | CA | C | 196 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(193): Show |
197 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(194): Show |
intron_variant | MODIFIER | c.163+16429delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102276525 | ||||||
chr10:102276525 | CAA | C | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(78): Show |
81 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.163+16428_163+1642 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102276525 | ||||||
chr10:102276525 | CAAAA | C | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+16426_163+1642 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102276525 | ||||||
chr10:102276540 | A | T | 1 | a0001c0001t0005g0152 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.163+16424A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102276540 | |||||||
chr10:102276593 | C | T | 1 | a0001c0001t0002g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.163+16477C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102276593 | |||||||
chr10:102276598 | G | A | 94 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(91): Show |
95 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.163+16482G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102276598 | |||||||
chr10:102276692 | T | A | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.163+16576T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102276692 | |||||||
chr10:102276958 | T | G | 22 | a0001c0001t0001g0208 a0001c0001t0001g0214 a0001c0001t0001g0215 others(19): Show |
22 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.163+16842T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102276958 | |||||||
chr10:102276965 | T | TAC | 13 | a0001c0001t0001g0158 a0001c0001t0001g0207 a0001c0001t0002g0035 others(10): Show |
13 | HG00280.hp1 HG00642.hp2 HG00738.hp1 others(10): Show |
intron_variant | MODIFIER | c.163+16875_163+1687 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102276965 | ||||||
chr10:102276965 | T | TACAC | 48 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0153 others(45): Show |
48 | HG00544.hp1 HG00609.hp2 HG01099.hp1 others(45): Show |
intron_variant | MODIFIER | c.163+16873_163+1687 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102276965 | ||||||
chr10:102276965 | TAC | T | 31 | a0001c0001t0001g0114 a0001c0001t0001g0208 a0001c0001t0001g0212 others(28): Show |
32 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(29): Show |
intron_variant | MODIFIER | c.163+16875_163+1687 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102276965 | ||||||
chr10:102276965 | TACAC | T | 4 | a0001c0001t0001g0184 a0001c0001t0001g0191 a0001c0001t0001g0195 others(1): Show |
4 | HG01928.hp1 HG01934.hp1 HG02273.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+16873_163+1687 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102276965 | ||||||
chr10:102277330 | G | T | 1 | a0001c0001t0002g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.163+17214G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102277330 | |||||||
chr10:102277392 | C | CT | 6 | a0001c0001t0001g0297 a0001c0001t0002g0019 a0001c0001t0003g0278 others(3): Show |
6 | HG02055.hp2 HG02451.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+17293dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102277392 | ||||||
chr10:102277392 | CT | C | 42 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(39): Show |
42 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.163+17293delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102277392 | ||||||
chr10:102277409 | T | C | 5 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+17293T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102277409 | |||||||
chr10:102277437 | T | C | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+17321T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102277437 | |||||||
chr10:102277527 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.163+17411C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102277527 | |||||||
chr10:102277576 | G | A | 7 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(4): Show |
7 | HG01106.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+17460G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102277576 | |||||||
chr10:102277668 | C | T | 25 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0212 others(22): Show |
25 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.163+17552C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102277668 | |||||||
chr10:102277987 | T | C | 6 | a0001c0001t0002g0018 a0001c0001t0002g0051 a0001c0001t0002g0058 others(3): Show |
6 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+17871T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102277987 | |||||||
chr10:102278275 | C | CT | 14 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0003g0231 others(11): Show |
15 | HG00280.hp1 HG00609.hp1 HG00609.hp2 others(12): Show |
intron_variant | MODIFIER | c.163+18173dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102278275 | ||||||
chr10:102278425 | A | G | 11 | a0001c0001t0001g0208 a0001c0001t0001g0214 a0001c0001t0001g0215 others(8): Show |
11 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.163+18309A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102278425 | |||||||
chr10:102278530 | G | T | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+18414G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102278530 | |||||||
chr10:102278660 | G | A | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+18544G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102278660 | |||||||
chr10:102278800 | T | C | 12 | a0001c0001t0003g0302 a0001c0001t0003g0303 a0001c0001t0003g0304 others(9): Show |
12 | HG00673.hp2 HG02071.hp2 HG02074.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+18684T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102278800 | |||||||
chr10:102279006 | T | G | 22 | a0001c0001t0001g0208 a0001c0001t0001g0214 a0001c0001t0001g0215 others(19): Show |
22 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.163+18890T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102279006 | |||||||
chr10:102279009 | A | G | 7 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(4): Show |
7 | HG01106.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+18893A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102279009 | |||||||
chr10:102279217 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.163+19101G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102279217 | |||||||
chr10:102279548 | G | A | 5 | a0001c0001t0003g0262 a0001c0001t0003g0283 a0001c0001t0003g0284 others(2): Show |
5 | NA18950.hp2 NA18979.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+19432G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102279548 | |||||||
chr10:102279717 | C | T | 1 | a0001c0001t0001g0246 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.163+19601C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102279717 | |||||||
chr10:102279750 | G | A | 1 | a0001c0001t0002g0088 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.163+19634G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102279750 | |||||||
chr10:102279958 | A | AT | 6 | a0001c0001t0002g0064 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+19851dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102279958 | ||||||
chr10:102280130 | A | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0136 a0001c0001t0001g0147 others(1): Show |
4 | NA18951.hp2 NA18964.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+20014A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102280130 | |||||||
chr10:102280519 | T | TAACAGAG others(614): Show |
1 | a0001c0001t0002g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.163+20418_163+2041 others(625): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102280519 | ||||||
chr10:102280557 | G | A | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+20441G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102280557 | |||||||
chr10:102280639 | G | A | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+20523G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102280639 | |||||||
chr10:102281581 | G | A | 320 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(317): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.163+21465G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102281581 | |||||||
chr10:102281949 | C | T | 6 | a0001c0003t0001g0206 a0001c0003t0001g0224 a0001c0003t0001g0226 others(3): Show |
6 | HG01081.hp1 HG02451.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+21833C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102281949 | |||||||
chr10:102281950 | A | G | 5 | a0001c0001t0002g0024 a0001c0001t0002g0035 a0001c0001t0002g0063 others(2): Show |
5 | HG00738.hp1 HG01074.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+21834A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102281950 | |||||||
chr10:102281966 | G | C | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+21850G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102281966 | |||||||
chr10:102282052 | G | T | 1 | a0001c0001t0005g0152 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.163+21936G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102282052 | |||||||
chr10:102282093 | AT | A | 11 | a0001c0001t0001g0185 a0001c0001t0001g0295 a0001c0001t0002g0066 others(8): Show |
12 | HG01256.hp2 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+21991delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102282093 | ||||||
chr10:102282093 | ATT | A | 90 | a0001c0001t0001g0159 a0001c0001t0002g0003 a0001c0001t0002g0004 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.163+21990_163+2199 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102282093 | ||||||
chr10:102282187 | G | A | 1 | a0001c0001t0002g0040 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.163+22071G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102282187 | |||||||
chr10:102282264 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.163+22148C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102282264 | |||||||
chr10:102282357 | G | A | 19 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(16): Show |
19 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.163+22241G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102282357 | |||||||
chr10:102282403 | G | A | 1 | a0001c0001t0002g0058 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.163+22287G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102282403 | |||||||
chr10:102282404 | A | G | 1 | a0001c0001t0002g0058 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.163+22288A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102282404 | |||||||
chr10:102282852 | G | A | 26 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0212 others(23): Show |
26 | HG01070.hp2 HG01074.hp1 HG01081.hp1 others(23): Show |
intron_variant | MODIFIER | c.163+22736G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102282852 | |||||||
chr10:102283258 | A | G | 25 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0212 others(22): Show |
25 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.163+23142A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102283258 | |||||||
chr10:102283329 | C | T | 1 | a0001c0001t0003g0257 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.163+23213C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102283329 | |||||||
chr10:102283759 | G | T | 29 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(26): Show |
29 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.163+23643G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102283759 | |||||||
chr10:102284061 | A | C | 2 | a0001c0001t0002g0029 a0001c0001t0002g0050 |
2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.163+23945A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102284061 | |||||||
chr10:102284088 | A | ACT | 118 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0109 others(115): Show |
119 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.163+23973_163+2397 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102284088 | ||||||
chr10:102284216 | AT | A | 4 | a0001c0001t0001g0230 a0001c0001t0001g0251 a0001c0001t0001g0252 others(1): Show |
4 | HG02922.hp1 HG03041.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+24102delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102284216 | ||||||
chr10:102284318 | A | G | 2 | a0001c0004t0002g0103 a0002c0002t0001g0104 |
2 | HG06807.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.163+24202A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102284318 | |||||||
chr10:102284580 | A | C | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+24464A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102284580 | |||||||
chr10:102284664 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.163+24548C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102284664 | |||||||
chr10:102284892 | G | T | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.163+24776G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102284892 | |||||||
chr10:102285175 | C | T | 12 | a0001c0001t0001g0131 a0001c0001t0001g0132 a0001c0001t0001g0139 others(9): Show |
12 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+25059C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102285175 | |||||||
chr10:102285425 | C | T | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+25309C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102285425 | |||||||
chr10:102286067 | G | C | 1 | a0001c0003t0001g0225 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.163+25951G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102286067 | |||||||
chr10:102286194 | G | GT | 11 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0115 others(8): Show |
11 | HG01891.hp1 HG01891.hp2 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.163+26101dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102286194 | ||||||
chr10:102286194 | GT | G | 92 | a0001c0001t0001g0012 a0001c0001t0001g0143 a0001c0001t0001g0151 others(89): Show |
92 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.163+26101delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102286194 | ||||||
chr10:102286202 | T | TG | 116 | a0001c0001t0001g0008 a0001c0001t0001g0109 a0001c0001t0001g0110 others(113): Show |
118 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(115): Show |
intron_variant | MODIFIER | c.163+26086_163+2608 others(5): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102286202 | |||||||
chr10:102286203 | T | G | 97 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0105 others(94): Show |
97 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.163+26087T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102286203 | |||||||
chr10:102286204 | T | G | 92 | a0001c0001t0001g0012 a0001c0001t0001g0143 a0001c0001t0001g0151 others(89): Show |
92 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.163+26088T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102286204 | |||||||
chr10:102286405 | T | G | 3 | a0001c0001t0003g0266 a0001c0001t0003g0275 a0001c0001t0003g0291 |
3 | NA18941.hp1 NA18967.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.163+26289T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102286405 | |||||||
chr10:102286662 | G | A | 1 | a0001c0007t0001g0328 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.163+26546G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102286662 | |||||||
chr10:102286725 | A | G | 1 | a0001c0001t0001g0296 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.163+26609A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102286725 | |||||||
chr10:102286871 | AGT | A | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.163+26757_163+2675 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102286871 | ||||||
chr10:102286969 | T | G | 1 | a0001c0001t0003g0260 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.163+26853T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102286969 | |||||||
chr10:102287283 | A | C | 1 | a0001c0001t0001g0161 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.163+27167A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102287283 | |||||||
chr10:102287339 | A | C | 7 | a0001c0001t0003g0262 a0001c0004t0002g0103 a0001c0004t0004g0001 others(4): Show |
8 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.163+27223A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102287339 | |||||||
chr10:102287344 | CT | C | 141 | a0001c0001t0001g0010 a0001c0001t0001g0109 a0001c0001t0001g0110 others(138): Show |
142 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(139): Show |
intron_variant | MODIFIER | c.163+27255delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102287344 | ||||||
chr10:102287344 | CTT | C | 12 | a0001c0001t0001g0009 a0001c0001t0001g0105 a0001c0001t0001g0158 others(9): Show |
12 | HG01258.hp2 HG02615.hp2 NA18959.hp1 others(9): Show |
intron_variant | MODIFIER | c.163+27254_163+2725 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102287344 | ||||||
chr10:102287344 | CTTTTTTT | C | 10 | a0001c0001t0001g0134 a0001c0001t0001g0162 a0001c0001t0001g0167 others(7): Show |
10 | HG01358.hp2 HG01928.hp1 HG02040.hp1 others(7): Show |
intron_variant | MODIFIER | c.163+27249_163+2725 others(11): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102287344 | ||||||
chr10:102287344 | CTTTTTTT others(1): Show |
C | 76 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(73): Show |
76 | HG00280.hp1 HG00544.hp1 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.163+27248_163+2725 others(12): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102287344 | ||||||
chr10:102287345 | T | A | 2 | a0001c0001t0002g0013 a0007c0011t0001g0294 |
2 | HG01074.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.163+27229T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102287345 | |||||||
chr10:102287350 | T | A | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.163+27234T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102287350 | |||||||
chr10:102287355 | T | A | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.163+27239T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102287355 | |||||||
chr10:102287401 | T | C | 1 | a0001c0001t0003g0276 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.163+27285T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102287401 | |||||||
chr10:102287472 | G | A | 1 | a0001c0001t0002g0064 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.163+27356G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102287472 | |||||||
chr10:102287795 | C | G | 29 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(26): Show |
29 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.163+27679C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102287795 | |||||||
chr10:102287862 | C | T | 25 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0212 others(22): Show |
25 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.163+27746C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102287862 | |||||||
chr10:102288079 | G | T | 57 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0017 others(54): Show |
57 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.163+27963G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288079 | |||||||
chr10:102288254 | T | G | 1 | a0001c0001t0001g0154 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.163+28138T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288254 | |||||||
chr10:102288327 | TATATAAT others(1): Show |
T | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.163+28224_163+2823 others(12): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102288327 | ||||||
chr10:102288438 | G | A | 4 | a0001c0001t0001g0230 a0001c0001t0001g0251 a0001c0001t0001g0252 others(1): Show |
4 | HG02922.hp1 HG03041.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+28322G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288438 | |||||||
chr10:102288480 | G | C | 3 | a0001c0001t0001g0110 a0001c0001t0001g0292 a0011c0010t0001g0112 |
3 | HG02615.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.163+28364G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288480 | |||||||
chr10:102288482 | C | A | 1 | a0001c0001t0003g0267 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.163+28366C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288482 | |||||||
chr10:102288482 | C | T | 1 | a0001c0001t0006g0164 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.163+28366C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288482 | |||||||
chr10:102288484 | G | A | 4 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 others(1): Show |
4 | NA18967.hp2 NA18977.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+28368G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288484 | |||||||
chr10:102288507 | C | T | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.163+28391C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288507 | |||||||
chr10:102288565 | GCCGGGCG others(20): Show |
G | 1 | a0001c0001t0001g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163+28452_163+2847 others(31): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102288565 | ||||||
chr10:102288712 | C | T | 1 | a0008c0018t0001g0204 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.163+28596C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288712 | |||||||
chr10:102288722 | G | GA | 42 | a0001c0001t0001g0117 a0001c0001t0001g0119 a0001c0001t0001g0134 others(39): Show |
42 | HG00099.hp2 HG00280.hp2 HG00738.hp1 others(39): Show |
intron_variant | MODIFIER | c.163+28619dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102288722 | ||||||
chr10:102288722 | G | GAA | 55 | a0001c0001t0002g0013 a0001c0001t0002g0018 a0001c0001t0002g0019 others(52): Show |
55 | HG00558.hp1 HG00621.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.163+28618_163+2861 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102288722 | ||||||
chr10:102288736 | C | A | 92 | a0001c0001t0001g0213 a0001c0001t0002g0003 a0001c0001t0002g0004 others(89): Show |
92 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(89): Show |
intron_variant | MODIFIER | c.163+28620C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288736 | |||||||
chr10:102288736 | C | CA | 80 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(77): Show |
81 | HG00544.hp1 HG00735.hp1 HG00735.hp2 others(78): Show |
intron_variant | MODIFIER | c.163+28632dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102288736 | ||||||
chr10:102288738 | A | AC | 3 | a0001c0001t0001g0139 a0001c0001t0001g0229 a0001c0001t0001g0321 |
3 | HG00621.hp1 HG02080.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.163+28622_163+2862 others(5): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288738 | |||||||
chr10:102288739 | A | C | 13 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0131 others(10): Show |
13 | HG00544.hp2 HG00558.hp2 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.163+28623A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288739 | |||||||
chr10:102288838 | C | T | 4 | a0001c0001t0003g0231 a0001c0001t0003g0232 a0001c0001t0003g0233 others(1): Show |
4 | HG00609.hp1 NA18959.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+28722C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102288838 | |||||||
chr10:102289105 | GA | G | 57 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0018 others(54): Show |
58 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(55): Show |
intron_variant | MODIFIER | c.163+29005delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102289105 | ||||||
chr10:102289105 | GAA | G | 37 | a0001c0001t0002g0004 a0001c0001t0002g0017 a0001c0001t0002g0028 others(34): Show |
37 | HG00558.hp1 HG00621.hp2 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.163+29004_163+2900 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102289105 | ||||||
chr10:102289393 | G | A | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.163+29277G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102289393 | |||||||
chr10:102289524 | A | T | 1 | a0001c0001t0002g0013 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.163+29408A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102289524 | |||||||
chr10:102289922 | C | T | 1 | a0001c0001t0003g0264 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.163+29806C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102289922 | |||||||
chr10:102289971 | C | T | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+29855C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102289971 | |||||||
chr10:102290027 | C | G | 6 | a0001c0001t0002g0027 a0001c0001t0002g0039 a0001c0001t0002g0040 others(3): Show |
6 | HG01934.hp2 HG01943.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+29911C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102290027 | |||||||
chr10:102290209 | C | T | 94 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(91): Show |
95 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.163+30093C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102290209 | |||||||
chr10:102290249 | G | A | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.163+30133G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102290249 | |||||||
chr10:102290263 | T | G | 1 | a0001c0001t0002g0049 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.163+30147T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102290263 | |||||||
chr10:102290422 | A | T | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+30306A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102290422 | |||||||
chr10:102290635 | A | G | 25 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0212 others(22): Show |
25 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.163+30519A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102290635 | |||||||
chr10:102291083 | A | C | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+30967A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102291083 | |||||||
chr10:102291140 | TTTTC | T | 25 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0212 others(22): Show |
25 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.163+31030_163+3103 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102291140 | ||||||
chr10:102291171 | C | CTTTG | 12 | a0001c0001t0001g0139 a0001c0001t0001g0141 a0001c0001t0001g0148 others(9): Show |
13 | HG00621.hp1 HG02027.hp2 HG02080.hp1 others(10): Show |
intron_variant | MODIFIER | c.163+31083_163+3108 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102291171 | ||||||
chr10:102291171 | C | T | 1 | a0001c0001t0001g0179 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.163+31055C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102291171 | |||||||
chr10:102291345 | T | C | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.163+31229T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102291345 | |||||||
chr10:102291408 | G | T | 3 | a0001c0001t0003g0002 a0001c0001t0003g0272 a0001c0001t0003g0278 |
4 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+31292G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102291408 | |||||||
chr10:102291667 | T | C | 325 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(322): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.163+31551T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102291667 | |||||||
chr10:102291728 | C | T | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+31612C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102291728 | |||||||
chr10:102291752 | G | A | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+31636G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102291752 | |||||||
chr10:102291890 | C | CT | 100 | a0001c0001t0001g0011 a0001c0001t0001g0136 a0001c0001t0001g0147 others(97): Show |
101 | HG00280.hp2 HG00558.hp1 HG00621.hp2 others(98): Show |
intron_variant | MODIFIER | c.163+31791dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102291890 | ||||||
chr10:102292141 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.163+32025G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102292141 | |||||||
chr10:102292187 | C | A | 1 | a0001c0001t0002g0063 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.163+32071C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102292187 | |||||||
chr10:102292315 | A | T | 1 | a0001c0001t0002g0073 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.163+32199A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102292315 | |||||||
chr10:102292349 | C | T | 1 | a0001c0001t0003g0264 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.163+32233C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102292349 | |||||||
chr10:102292660 | G | A | 1 | a0001c0001t0002g0299 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.163+32544G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102292660 | |||||||
chr10:102292811 | G | A | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+32695G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102292811 | |||||||
chr10:102292936 | A | G | 1 | a0001c0003t0001g0206 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.163+32820A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102292936 | |||||||
chr10:102293102 | G | A | 3 | a0001c0001t0001g0110 a0001c0001t0001g0292 a0011c0010t0001g0112 |
3 | HG02615.hp1 HG02818.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.163+32986G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102293102 | |||||||
chr10:102293400 | TTATC | T | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.163+33288_163+3329 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293400 | ||||||
chr10:102293584 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.163+33468C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102293584 | |||||||
chr10:102293623 | C | G | 1 | a0001c0001t0001g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163+33507C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102293623 | |||||||
chr10:102293762 | ATGTTTTG | A | 4 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0016 others(1): Show |
5 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+33653_163+3365 others(11): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293762 | ||||||
chr10:102293764 | G | GT | 3 | a0001c0001t0001g0161 a0005c0006t0001g0156 a0005c0006t0001g0157 |
3 | HG00544.hp1 HG02135.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.163+33652dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | G | GTTTT | 11 | a0001c0001t0001g0012 a0001c0001t0001g0131 a0001c0001t0001g0143 others(8): Show |
11 | HG00738.hp2 HG01192.hp2 HG01978.hp1 others(8): Show |
intron_variant | MODIFIER | c.163+33649_163+3365 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | G | GTTTTT | 32 | a0001c0001t0001g0006 a0001c0001t0001g0132 a0001c0001t0001g0133 others(29): Show |
32 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(29): Show |
intron_variant | MODIFIER | c.163+33652_163+3365 others(9): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | G | GTTTTTT | 31 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0149 others(28): Show |
31 | HG00280.hp2 HG00558.hp1 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.163+33652_163+3365 others(10): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | G | GTTTTTTT | 31 | a0001c0001t0001g0113 a0001c0001t0001g0140 a0001c0001t0001g0207 others(28): Show |
31 | HG00099.hp2 HG00673.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.163+33652_163+3365 others(11): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | G | GTTTTTTT others(1): Show |
18 | a0001c0001t0002g0034 a0001c0001t0002g0038 a0001c0001t0002g0041 others(15): Show |
18 | HG00621.hp2 HG01516.hp2 HG01928.hp2 others(15): Show |
intron_variant | MODIFIER | c.163+33652_163+3365 others(12): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | G | GTTTTTTT others(2): Show |
12 | a0001c0001t0002g0027 a0001c0001t0002g0039 a0001c0001t0002g0040 others(9): Show |
12 | HG01934.hp2 HG02027.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.163+33652_163+3365 others(13): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | G | GTTTTTTT others(3): Show |
2 | a0001c0001t0001g0136 a0001c0001t0001g0147 |
2 | NA18964.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.163+33652_163+3365 others(14): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | G | GTTTTTTT others(5): Show |
1 | a0002c0002t0001g0104 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.163+33652_163+3365 others(16): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | G | GTTTTTTT others(6): Show |
3 | a0002c0002t0001g0107 a0002c0002t0001g0171 a0002c0002t0001g0202 |
3 | HG01099.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.163+33652_163+3365 others(17): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | G | GTTTTTTT others(7): Show |
6 | a0001c0001t0001g0106 a0001c0001t0001g0167 a0001c0001t0001g0179 others(3): Show |
6 | HG01123.hp1 HG01981.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+33652_163+3365 others(18): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | G | GTTTTTTT others(8): Show |
8 | a0001c0001t0001g0011 a0001c0001t0001g0163 a0001c0001t0001g0175 others(5): Show |
8 | HG00735.hp2 HG01175.hp1 HG01361.hp1 others(5): Show |
intron_variant | MODIFIER | c.163+33652_163+3365 others(19): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | G | GTTTTTTT others(9): Show |
7 | a0001c0001t0001g0162 a0001c0001t0001g0180 a0001c0001t0001g0183 others(4): Show |
7 | HG00609.hp2 HG02683.hp2 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.163+33652_163+3365 others(20): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | G | GTTTTTTT others(10): Show |
3 | a0001c0001t0001g0105 a0001c0001t0001g0173 a0001c0001t0005g0155 |
3 | HG00280.hp1 NA18945.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.163+33652_163+3365 others(21): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | G | GTTTTTTT others(11): Show |
2 | a0001c0001t0001g0160 a0001c0001t0006g0164 |
2 | HG02293.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.163+33652_163+3365 others(22): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | G | GTTTTTTT others(14): Show |
4 | a0001c0001t0001g0008 a0001c0001t0001g0170 a0001c0001t0001g0182 others(1): Show |
4 | HG03471.hp2 HG04204.hp1 NA18974.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+33652_163+3365 others(25): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | G | GTTTTTTT others(15): Show |
2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | NA18971.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.163+33652_163+3365 others(26): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | G | GTTTTTTT others(16): Show |
3 | a0001c0001t0001g0159 a0001c0001t0001g0197 a0002c0002t0001g0198 |
3 | HG01258.hp1 NA18982.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.163+33652_163+3365 others(27): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | G | GTTTTTTT others(17): Show |
1 | a0002c0002t0001g0177 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.163+33652_163+3365 others(28): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | GTTTTGTG others(4): Show |
G | 4 | a0001c0001t0003g0260 a0001c0001t0003g0312 a0001c0001t0003g0315 others(1): Show |
4 | HG00741.hp1 HG02148.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.163+33653_163+3366 others(15): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | GTTTTGTG others(5): Show |
G | 103 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0109 others(100): Show |
104 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.163+33653_163+3366 others(16): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | GTTTTGTG others(6): Show |
G | 7 | a0001c0001t0001g0110 a0001c0001t0001g0111 a0001c0001t0001g0126 others(4): Show |
7 | HG01169.hp1 HG02615.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+33653_163+3366 others(17): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | GTTTTGTG others(7): Show |
G | 2 | a0004c0008t0001g0194 a0004c0008t0001g0199 |
2 | NA18949.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.163+33653_163+3366 others(18): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293764 | GTTTTGTG others(8): Show |
G | 10 | a0001c0001t0001g0153 a0001c0001t0001g0174 a0001c0001t0001g0178 others(7): Show |
10 | HG01928.hp1 HG01934.hp1 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.163+33653_163+3366 others(19): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293764 | ||||||
chr10:102293765 | TTTTGTG | T | 6 | a0001c0004t0002g0103 a0001c0004t0004g0014 a0003c0005t0002g0076 others(3): Show |
6 | HG01074.hp1 HG06807.hp1 NA18952.hp1 others(3): Show |
intron_variant | MODIFIER | c.163+33653_163+3365 others(10): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102293765 | ||||||
chr10:102293769 | G | T | 182 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0011 others(179): Show |
182 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(179): Show |
intron_variant | MODIFIER | c.163+33653G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102293769 | |||||||
chr10:102293771 | G | T | 183 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0011 others(180): Show |
183 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(180): Show |
intron_variant | MODIFIER | c.163+33655G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102293771 | |||||||
chr10:102293838 | C | T | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.163+33722C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102293838 | |||||||
chr10:102293955 | T | G | 2 | a0001c0001t0003g0201 a0001c0023t0003g0269 |
2 | HG01106.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.163+33839T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102293955 | |||||||
chr10:102294152 | A | G | 1 | a0001c0001t0002g0075 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.163+34036A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102294152 | |||||||
chr10:102294257 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.163+34141G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102294257 | |||||||
chr10:102294386 | C | CT | 86 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(83): Show |
86 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.163+34283dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102294386 | ||||||
chr10:102294526 | C | T | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+34410C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102294526 | |||||||
chr10:102294621 | C | T | 5 | a0001c0003t0001g0108 a0001c0003t0001g0209 a0001c0003t0001g0210 others(2): Show |
5 | HG01070.hp2 HG01516.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+34505C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102294621 | |||||||
chr10:102294671 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.163+34555C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102294671 | |||||||
chr10:102294707 | G | A | 1 | a0001c0001t0002g0102 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.163+34591G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102294707 | |||||||
chr10:102294848 | T | C | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+34732T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102294848 | |||||||
chr10:102294860 | C | T | 2 | a0001c0001t0002g0029 a0001c0001t0002g0050 |
2 | HG02258.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.163+34744C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102294860 | |||||||
chr10:102295361 | A | G | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+35245A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102295361 | |||||||
chr10:102295799 | C | T | 18 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(15): Show |
18 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.163+35683C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102295799 | |||||||
chr10:102295831 | A | AT | 5 | a0001c0001t0003g0250 a0001c0001t0003g0266 a0001c0001t0003g0275 others(2): Show |
5 | NA18941.hp1 NA18967.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.163+35717dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102295831 | ||||||
chr10:102295955 | T | C | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+35839T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102295955 | |||||||
chr10:102296159 | A | G | 1 | a0001c0001t0002g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.163+36043A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102296159 | |||||||
chr10:102296226 | A | G | 55 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(52): Show |
55 | HG00544.hp1 HG00609.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.163+36110A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102296226 | |||||||
chr10:102296511 | A | G | 94 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(91): Show |
95 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.163+36395A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102296511 | |||||||
chr10:102296610 | C | T | 4 | a0001c0001t0002g0017 a0001c0001t0002g0034 a0009c0019t0002g0042 others(1): Show |
4 | HG01928.hp2 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+36494C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102296610 | |||||||
chr10:102296671 | G | A | 29 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(26): Show |
29 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.163+36555G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102296671 | |||||||
chr10:102296709 | C | T | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.163+36593C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102296709 | |||||||
chr10:102297057 | G | A | 1 | a0003c0005t0002g0101 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.163+36941G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102297057 | |||||||
chr10:102297057 | G | GA | 86 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(83): Show |
86 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(83): Show |
intron_variant | MODIFIER | c.163+36949dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102297057 | ||||||
chr10:102297153 | C | T | 1 | a0001c0001t0002g0034 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.163+37037C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102297153 | |||||||
chr10:102297195 | T | C | 4 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0138 others(1): Show |
4 | HG00642.hp1 HG00738.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+37079T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102297195 | |||||||
chr10:102297335 | T | C | 1 | a0001c0001t0002g0017 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.163+37219T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102297335 | |||||||
chr10:102297494 | A | C | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.163+37378A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102297494 | |||||||
chr10:102297724 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.163+37608A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102297724 | |||||||
chr10:102297916 | A | G | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+37800A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102297916 | |||||||
chr10:102297931 | G | T | 94 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(91): Show |
95 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.163+37815G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102297931 | |||||||
chr10:102297939 | G | T | 4 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0050 others(1): Show |
4 | HG02258.hp2 HG02647.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+37823G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102297939 | |||||||
chr10:102297959 | G | A | 1 | a0005c0006t0001g0156 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.163+37843G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102297959 | |||||||
chr10:102298007 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.163+37891T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102298007 | |||||||
chr10:102298030 | T | G | 325 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(322): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.163+37914T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102298030 | |||||||
chr10:102298037 | T | C | 320 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(317): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.163+37921T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102298037 | |||||||
chr10:102298042 | C | G | 1 | a0002c0002t0001g0172 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.163+37926C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102298042 | |||||||
chr10:102298115 | A | G | 1 | a0001c0003t0001g0224 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.163+37999A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102298115 | |||||||
chr10:102298441 | G | A | 1 | a0001c0024t0001g0228 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.163+38325G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102298441 | |||||||
chr10:102298495 | C | G | 1 | a0001c0001t0001g0126 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.163+38379C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102298495 | |||||||
chr10:102298764 | G | A | 2 | a0001c0001t0002g0051 a0001c0001t0002g0062 |
2 | HG00280.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.163+38648G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102298764 | |||||||
chr10:102298880 | C | G | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.163+38764C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102298880 | |||||||
chr10:102299238 | T | C | 5 | a0001c0001t0001g0230 a0001c0001t0001g0251 a0001c0001t0001g0252 others(2): Show |
5 | HG02922.hp1 HG03041.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.163+39122T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102299238 | |||||||
chr10:102299382 | A | G | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.163+39266A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102299382 | |||||||
chr10:102299409 | G | C | 1 | a0001c0001t0001g0180 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.163+39293G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102299409 | |||||||
chr10:102299545 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.163+39429C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102299545 | |||||||
chr10:102299636 | G | A | 4 | a0001c0001t0002g0017 a0001c0001t0002g0034 a0009c0019t0002g0042 others(1): Show |
4 | HG01928.hp2 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.163+39520G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102299636 | |||||||
chr10:102299659 | G | A | 320 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(317): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.163+39543G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102299659 | |||||||
chr10:102299741 | G | C | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+39625G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102299741 | |||||||
chr10:102299983 | A | G | 1 | a0001c0001t0002g0004 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.163+39867A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102299983 | |||||||
chr10:102300303 | G | C | 77 | a0001c0001t0001g0190 a0001c0001t0001g0240 a0001c0001t0001g0242 others(74): Show |
78 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.163+40187G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102300303 | |||||||
chr10:102300772 | C | T | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.163+40656C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102300772 | |||||||
chr10:102300976 | C | CT | 226 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(223): Show |
226 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.163+40876dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102300976 | ||||||
chr10:102300976 | C | CTT | 11 | a0001c0001t0001g0008 a0001c0001t0001g0169 a0001c0001t0002g0064 others(8): Show |
12 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.163+40875_163+4087 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102300976 | ||||||
chr10:102300999 | T | A | 49 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0018 others(46): Show |
49 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.163+40883T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102300999 | |||||||
chr10:102301063 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.163+40947A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301063 | |||||||
chr10:102301269 | C | T | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.163+41153C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301269 | |||||||
chr10:102301323 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.163+41207C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301323 | |||||||
chr10:102301339 | T | C | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.163+41223T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301339 | |||||||
chr10:102301368 | T | C | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.163+41252T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301368 | |||||||
chr10:102301461 | C | T | 2 | a0001c0001t0002g0083 a0001c0001t0002g0084 |
2 | HG00741.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.163+41345C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301461 | |||||||
chr10:102301462 | G | A | 88 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0190 others(85): Show |
89 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(86): Show |
intron_variant | MODIFIER | c.163+41346G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301462 | |||||||
chr10:102301521 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.163+41405G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301521 | |||||||
chr10:102301625 | C | T | 1 | a0005c0006t0001g0156 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.163+41509C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301625 | |||||||
chr10:102301785 | G | T | 1 | a0001c0013t0002g0048 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.163+41669G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301785 | |||||||
chr10:102301853 | C | T | 1 | a0001c0001t0003g0314 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.163+41737C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301853 | |||||||
chr10:102301949 | C | T | 1 | a0001c0001t0002g0068 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.163+41833C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102301949 | |||||||
chr10:102302038 | A | G | 1 | a0001c0001t0001g0006 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.163+41922A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302038 | |||||||
chr10:102302134 | G | A | 1 | a0001c0001t0002g0004 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.164-41917G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302134 | |||||||
chr10:102302191 | T | C | 1 | a0001c0001t0003g0284 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.164-41860T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302191 | |||||||
chr10:102302251 | TGTGGAAA others(5): Show |
T | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.164-41799_164-4178 others(16): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302251 | |||||||
chr10:102302460 | C | T | 1 | a0001c0001t0003g0272 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.164-41591C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302460 | |||||||
chr10:102302657 | A | G | 1 | a0001c0001t0001g0300 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.164-41394A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302657 | |||||||
chr10:102302678 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.164-41373A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302678 | |||||||
chr10:102302735 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.164-41316A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302735 | |||||||
chr10:102302737 | A | G | 121 | a0001c0001t0001g0154 a0001c0001t0001g0207 a0001c0001t0001g0208 others(118): Show |
122 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.164-41314A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302737 | |||||||
chr10:102302847 | G | A | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-41204G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302847 | |||||||
chr10:102302931 | A | G | 320 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(317): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.164-41120A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102302931 | |||||||
chr10:102302986 | C | CT | 43 | a0001c0001t0001g0123 a0001c0001t0001g0132 a0001c0001t0001g0136 others(40): Show |
44 | HG00544.hp2 HG00558.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.164-41047dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102302986 | ||||||
chr10:102303005 | G | A | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-41046G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102303005 | |||||||
chr10:102303118 | G | A | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-40933G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102303118 | |||||||
chr10:102303458 | G | A | 1 | a0001c0001t0002g0102 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.164-40593G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102303458 | |||||||
chr10:102303610 | A | G | 94 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(91): Show |
95 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.164-40441A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102303610 | |||||||
chr10:102303730 | C | A | 5 | a0001c0001t0002g0021 a0001c0001t0002g0052 a0001c0001t0002g0054 others(2): Show |
5 | NA18951.hp1 NA18968.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-40321C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102303730 | |||||||
chr10:102303796 | A | G | 3 | a0001c0001t0006g0164 a0001c0001t0006g0165 a0012c0017t0001g0192 |
3 | HG03017.hp1 HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.164-40255A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102303796 | |||||||
chr10:102303800 | T | A | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-40251T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102303800 | |||||||
chr10:102303860 | A | G | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-40191A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102303860 | |||||||
chr10:102303990 | G | GT | 7 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(4): Show |
7 | HG01106.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-40051dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102303990 | ||||||
chr10:102304094 | T | C | 4 | a0001c0001t0002g0086 a0001c0001t0002g0087 a0001c0001t0002g0088 others(1): Show |
4 | HG00558.hp1 HG00621.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-39957T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102304094 | |||||||
chr10:102304287 | C | T | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-39764C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102304287 | |||||||
chr10:102304345 | C | T | 29 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(26): Show |
29 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(26): Show |
intron_variant | MODIFIER | c.164-39706C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102304345 | |||||||
chr10:102304493 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.164-39558G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102304493 | |||||||
chr10:102304791 | A | G | 113 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0109 others(110): Show |
114 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(111): Show |
intron_variant | MODIFIER | c.164-39260A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102304791 | |||||||
chr10:102304989 | AAAAG | A | 5 | a0001c0001t0001g0006 a0001c0001t0001g0136 a0001c0001t0001g0147 others(2): Show |
5 | HG01175.hp2 HG02074.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-39034_164-3903 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102304989 | ||||||
chr10:102304989 | AAAAGAAA others(1): Show |
A | 319 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(316): Show |
321 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.164-39038_164-3903 others(12): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102304989 | ||||||
chr10:102305089 | C | A | 325 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(322): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.164-38962C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102305089 | |||||||
chr10:102305128 | C | G | 94 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(91): Show |
95 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.164-38923C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102305128 | |||||||
chr10:102305175 | T | TTG | 20 | a0001c0001t0001g0122 a0001c0001t0001g0208 a0001c0001t0001g0217 others(17): Show |
21 | HG01070.hp1 HG01070.hp2 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.164-38832_164-3883 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305175 | ||||||
chr10:102305175 | T | TTGTG | 5 | a0001c0001t0001g0117 a0001c0001t0001g0218 a0001c0001t0002g0040 others(2): Show |
5 | HG01934.hp2 HG02698.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-38834_164-3883 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305175 | ||||||
chr10:102305175 | T | TTGTGTGT others(1): Show |
6 | a0001c0001t0001g0154 a0001c0001t0001g0213 a0001c0004t0004g0001 others(3): Show |
6 | HG02055.hp1 HG02486.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-38838_164-3883 others(12): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305175 | ||||||
chr10:102305175 | T | TTGTGTGT others(5): Show |
1 | a0001c0004t0004g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.164-38842_164-3883 others(16): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305175 | ||||||
chr10:102305175 | TTG | T | 65 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0114 others(62): Show |
65 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(62): Show |
intron_variant | MODIFIER | c.164-38832_164-3883 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305175 | ||||||
chr10:102305175 | TTGTG | T | 156 | a0001c0001t0001g0006 a0001c0001t0001g0106 a0001c0001t0001g0110 others(153): Show |
156 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(153): Show |
intron_variant | MODIFIER | c.164-38834_164-3883 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305175 | ||||||
chr10:102305175 | TTGTGTG | T | 36 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(33): Show |
36 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.164-38836_164-3883 others(10): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305175 | ||||||
chr10:102305175 | TTGTGTGT others(1): Show |
T | 3 | a0001c0001t0001g0136 a0001c0001t0002g0085 a0001c0001t0002g0096 |
3 | HG03942.hp2 HG04184.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.164-38838_164-3883 others(12): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305175 | ||||||
chr10:102305175 | TTGTGTGT others(3): Show |
T | 1 | a0001c0001t0001g0229 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.164-38840_164-3883 others(14): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305175 | ||||||
chr10:102305175 | TTGTGTGT others(5): Show |
T | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-38842_164-3883 others(16): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305175 | ||||||
chr10:102305472 | T | C | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-38579T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102305472 | |||||||
chr10:102305488 | T | C | 1 | a0001c0001t0001g0240 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.164-38563T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102305488 | |||||||
chr10:102305540 | G | T | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-38511G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102305540 | |||||||
chr10:102305610 | C | CA | 9 | a0001c0001t0002g0036 a0001c0001t0002g0045 a0001c0004t0002g0103 others(6): Show |
10 | HG01074.hp1 HG01358.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.164-38431dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102305610 | ||||||
chr10:102305771 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.164-38280C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102305771 | |||||||
chr10:102305983 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.164-38068A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102305983 | |||||||
chr10:102306046 | C | CTA | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.164-37994_164-3799 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102306046 | ||||||
chr10:102306360 | C | A | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.164-37691C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102306360 | |||||||
chr10:102306463 | G | A | 5 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-37588G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102306463 | |||||||
chr10:102306480 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.164-37571A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102306480 | |||||||
chr10:102306482 | G | A | 28 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(25): Show |
28 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.164-37569G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102306482 | |||||||
chr10:102306615 | G | C | 2 | a0001c0001t0001g0012 a0001c0001t0001g0151 |
2 | HG00738.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.164-37436G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102306615 | |||||||
chr10:102306650 | C | T | 2 | a0001c0001t0002g0097 a0001c0001t0002g0299 |
2 | NA18961.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.164-37401C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102306650 | |||||||
chr10:102306750 | A | T | 55 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(52): Show |
55 | HG00544.hp1 HG00609.hp2 HG00735.hp2 others(52): Show |
intron_variant | MODIFIER | c.164-37301A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102306750 | |||||||
chr10:102306883 | A | G | 320 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(317): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.164-37168A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102306883 | |||||||
chr10:102306945 | T | C | 1 | a0001c0001t0001g0186 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.164-37106T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102306945 | |||||||
chr10:102306951 | ATC | A | 5 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0001g0123 others(2): Show |
5 | HG01891.hp2 HG02965.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-37098_164-3709 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102306951 | ||||||
chr10:102307100 | T | G | 1 | a0001c0001t0001g0154 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.164-36951T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307100 | |||||||
chr10:102307228 | A | C | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-36823A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307228 | |||||||
chr10:102307246 | T | C | 4 | a0001c0001t0002g0017 a0001c0001t0002g0034 a0009c0019t0002g0042 others(1): Show |
4 | HG01928.hp2 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-36805T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307246 | |||||||
chr10:102307266 | A | G | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.164-36785A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307266 | |||||||
chr10:102307443 | C | CA | 10 | a0001c0001t0001g0190 a0001c0001t0001g0246 a0001c0001t0001g0321 others(7): Show |
10 | HG00609.hp1 HG01358.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.164-36592dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102307443 | ||||||
chr10:102307461 | G | T | 1 | a0001c0001t0001g0251 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.164-36590G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307461 | |||||||
chr10:102307476 | G | A | 2 | a0001c0001t0002g0020 a0001c0001t0002g0037 |
2 | HG00099.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.164-36575G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307476 | |||||||
chr10:102307682 | C | T | 6 | a0001c0001t0002g0027 a0001c0001t0002g0039 a0001c0001t0002g0040 others(3): Show |
6 | HG01934.hp2 HG01943.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-36369C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307682 | |||||||
chr10:102307734 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.164-36317G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307734 | |||||||
chr10:102307829 | A | G | 1 | a0002c0002t0001g0198 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.164-36222A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307829 | |||||||
chr10:102307831 | T | C | 4 | a0001c0001t0002g0086 a0001c0001t0002g0087 a0001c0001t0002g0088 others(1): Show |
4 | HG00558.hp1 HG00621.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-36220T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307831 | |||||||
chr10:102307889 | A | C | 1 | a0001c0001t0002g0004 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.164-36162A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102307889 | |||||||
chr10:102308201 | T | TA | 163 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(160): Show |
165 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(162): Show |
intron_variant | MODIFIER | c.164-35832dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102308201 | ||||||
chr10:102308201 | T | TAA | 66 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(63): Show |
66 | HG00544.hp1 HG00735.hp2 HG00741.hp1 others(63): Show |
intron_variant | MODIFIER | c.164-35833_164-3583 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102308201 | ||||||
chr10:102308201 | T | TAAA | 83 | a0001c0001t0001g0186 a0001c0001t0002g0003 a0001c0001t0002g0004 others(80): Show |
83 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.164-35834_164-3583 others(7): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102308201 | ||||||
chr10:102308280 | A | G | 1 | a0001c0001t0002g0036 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.164-35771A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102308280 | |||||||
chr10:102308290 | A | T | 5 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0022 others(2): Show |
5 | HG00099.hp2 HG01255.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-35761A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102308290 | |||||||
chr10:102308381 | A | G | 2 | a0001c0001t0002g0083 a0001c0001t0002g0084 |
2 | HG00741.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.164-35670A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102308381 | |||||||
chr10:102308633 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.164-35418C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102308633 | |||||||
chr10:102308739 | G | A | 83 | a0001c0001t0001g0190 a0001c0001t0001g0230 a0001c0001t0001g0236 others(80): Show |
84 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(81): Show |
intron_variant | MODIFIER | c.164-35312G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102308739 | |||||||
chr10:102309164 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.164-34887C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102309164 | |||||||
chr10:102309700 | C | T | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-34351C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102309700 | |||||||
chr10:102309701 | T | A | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-34350T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102309701 | |||||||
chr10:102309707 | T | C | 1 | a0001c0001t0002g0064 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.164-34344T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102309707 | |||||||
chr10:102309839 | C | A | 1 | a0001c0001t0002g0088 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.164-34212C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102309839 | |||||||
chr10:102310259 | A | G | 22 | a0001c0001t0001g0208 a0001c0001t0001g0214 a0001c0001t0001g0215 others(19): Show |
22 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.164-33792A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102310259 | |||||||
chr10:102310927 | G | A | 1 | a0001c0001t0002g0038 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.164-33124G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102310927 | |||||||
chr10:102311295 | G | A | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-32756G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102311295 | |||||||
chr10:102311338 | T | A | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-32713T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102311338 | |||||||
chr10:102311431 | T | C | 1 | a0001c0001t0002g0039 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.164-32620T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102311431 | |||||||
chr10:102311460 | A | G | 1 | a0001c0001t0001g0296 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.164-32591A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102311460 | |||||||
chr10:102311725 | C | G | 1 | a0001c0001t0001g0141 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.164-32326C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102311725 | |||||||
chr10:102312044 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.164-32007C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102312044 | |||||||
chr10:102312216 | C | G | 57 | a0001c0001t0002g0003 a0001c0001t0002g0013 a0001c0001t0002g0017 others(54): Show |
57 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.164-31835C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102312216 | |||||||
chr10:102312295 | G | GA | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-31741dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102312295 | ||||||
chr10:102312295 | GA | G | 32 | a0001c0001t0001g0126 a0001c0001t0002g0004 a0001c0001t0002g0026 others(29): Show |
32 | HG00558.hp1 HG00621.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.164-31741delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102312295 | ||||||
chr10:102312538 | G | A | 2 | a0001c0001t0001g0297 a0001c0001t0001g0298 |
2 | HG02559.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.164-31513G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102312538 | |||||||
chr10:102312570 | T | C | 96 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(93): Show |
97 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.164-31481T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102312570 | |||||||
chr10:102312609 | GGTTAAAA others(7): Show |
G | 1 | a0001c0001t0005g0152 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.164-31424_164-3141 others(18): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102312609 | ||||||
chr10:102312699 | C | T | 3 | a0001c0001t0003g0260 a0001c0001t0003g0268 a0001c0001t0003g0270 |
3 | HG00735.hp1 HG00741.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.164-31352C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102312699 | |||||||
chr10:102313014 | G | A | 1 | a0001c0001t0001g0138 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.164-31037G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102313014 | |||||||
chr10:102313090 | C | T | 2 | a0001c0001t0003g0274 a0001c0001t0003g0281 |
2 | NA19079.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.164-30961C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102313090 | |||||||
chr10:102313207 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.164-30844G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102313207 | |||||||
chr10:102313358 | AC | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0065 a0001c0001t0002g0066 |
3 | HG01069.hp2 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.164-30691delC | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102313358 | ||||||
chr10:102313363 | C | T | 1 | a0001c0001t0002g0029 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.164-30688C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102313363 | |||||||
chr10:102313692 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.164-30359C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102313692 | |||||||
chr10:102314020 | A | G | 6 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0028 others(3): Show |
6 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-30031A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314020 | |||||||
chr10:102314075 | A | G | 1 | a0001c0024t0001g0228 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.164-29976A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314075 | |||||||
chr10:102314141 | C | CT | 126 | a0001c0001t0001g0138 a0001c0001t0001g0153 a0001c0001t0001g0161 others(123): Show |
126 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.164-29891dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102314141 | ||||||
chr10:102314141 | C | CTT | 16 | a0001c0001t0001g0008 a0001c0001t0001g0158 a0001c0001t0002g0036 others(13): Show |
16 | HG00738.hp1 HG01358.hp1 HG02071.hp1 others(13): Show |
intron_variant | MODIFIER | c.164-29892_164-2989 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102314141 | ||||||
chr10:102314141 | C | CTTTT | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-29894_164-2989 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102314141 | ||||||
chr10:102314301 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.164-29750C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314301 | |||||||
chr10:102314302 | A | G | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-29749A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314302 | |||||||
chr10:102314308 | C | G | 16 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0131 others(13): Show |
16 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.164-29743C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314308 | |||||||
chr10:102314318 | A | AT | 8 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(5): Show |
8 | HG01891.hp2 HG02145.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-29725dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102314318 | ||||||
chr10:102314394 | G | A | 5 | a0001c0001t0001g0119 a0001c0001t0001g0126 a0001c0001t0001g0127 others(2): Show |
5 | HG02280.hp2 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-29657G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314394 | |||||||
chr10:102314398 | A | C | 1 | a0001c0001t0001g0006 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.164-29653A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314398 | |||||||
chr10:102314398 | A | T | 90 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.164-29653A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314398 | |||||||
chr10:102314519 | G | A | 1 | a0003c0005t0002g0060 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.164-29532G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314519 | |||||||
chr10:102314565 | T | A | 96 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(93): Show |
97 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.164-29486T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314565 | |||||||
chr10:102314583 | G | T | 16 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0131 others(13): Show |
16 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.164-29468G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314583 | |||||||
chr10:102314815 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.164-29236G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314815 | |||||||
chr10:102314935 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.164-29116A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102314935 | |||||||
chr10:102315138 | G | A | 1 | a0001c0004t0004g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.164-28913G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102315138 | |||||||
chr10:102315308 | C | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0065 a0001c0001t0002g0066 |
3 | HG01069.hp2 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.164-28743C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102315308 | |||||||
chr10:102315337 | G | T | 1 | a0001c0001t0002g0024 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.164-28714G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102315337 | |||||||
chr10:102315460 | A | G | 114 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0109 others(111): Show |
115 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(112): Show |
intron_variant | MODIFIER | c.164-28591A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102315460 | |||||||
chr10:102315554 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.164-28497C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102315554 | |||||||
chr10:102315651 | T | G | 1 | a0001c0001t0003g0289 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.164-28400T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102315651 | |||||||
chr10:102315784 | T | G | 96 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(93): Show |
97 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.164-28267T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102315784 | |||||||
chr10:102315861 | A | G | 6 | a0001c0001t0001g0214 a0001c0001t0001g0215 a0001c0001t0001g0217 others(3): Show |
6 | HG02559.hp2 HG02970.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-28190A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102315861 | |||||||
chr10:102315863 | TA | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0136 a0001c0001t0001g0147 |
3 | NA18964.hp1 NA18992.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.164-28187delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102315863 | |||||||
chr10:102315964 | T | C | 90 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.164-28087T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102315964 | |||||||
chr10:102316084 | C | CT | 17 | a0001c0001t0001g0117 a0001c0001t0001g0149 a0001c0001t0001g0163 others(14): Show |
18 | HG01099.hp1 HG01109.hp1 HG01361.hp1 others(15): Show |
intron_variant | MODIFIER | c.164-27947dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102316084 | ||||||
chr10:102316084 | CT | C | 8 | a0001c0001t0001g0106 a0001c0001t0001g0186 a0001c0001t0001g0242 others(5): Show |
8 | HG00099.hp2 HG01070.hp2 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-27947delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102316084 | ||||||
chr10:102316179 | T | C | 98 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(95): Show |
99 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(96): Show |
intron_variant | MODIFIER | c.164-27872T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316179 | |||||||
chr10:102316188 | G | A | 1 | a0001c0022t0003g0234 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.164-27863G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316188 | |||||||
chr10:102316268 | G | A | 90 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.164-27783G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316268 | |||||||
chr10:102316277 | G | A | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-27774G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316277 | |||||||
chr10:102316282 | T | C | 23 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0214 others(20): Show |
23 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.164-27769T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316282 | |||||||
chr10:102316293 | G | A | 4 | a0001c0001t0001g0105 a0001c0001t0001g0158 a0001c0001t0001g0160 others(1): Show |
4 | HG02293.hp2 NA18954.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-27758G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316293 | |||||||
chr10:102316335 | C | T | 10 | a0001c0001t0001g0208 a0001c0001t0001g0214 a0001c0001t0001g0215 others(7): Show |
10 | HG02145.hp1 HG02559.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.164-27716C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316335 | |||||||
chr10:102316380 | G | A | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-27671G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316380 | |||||||
chr10:102316474 | G | A | 59 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(56): Show |
59 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.164-27577G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316474 | |||||||
chr10:102316480 | C | T | 1 | a0001c0001t0002g0038 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.164-27571C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316480 | |||||||
chr10:102316780 | G | A | 2 | a0001c0001t0003g0302 a0001c0001t0003g0303 |
2 | HG02071.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.164-27271G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316780 | |||||||
chr10:102316802 | C | A | 1 | a0001c0001t0002g0036 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.164-27249C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102316802 | |||||||
chr10:102317021 | T | C | 1 | a0001c0001t0001g0200 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.164-27030T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102317021 | |||||||
chr10:102317182 | AGCTACTC others(5): Show |
A | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-26865_164-2685 others(16): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102317182 | ||||||
chr10:102317199 | A | G | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-26852A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102317199 | |||||||
chr10:102317211 | C | T | 1 | a0001c0001t0002g0022 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.164-26840C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102317211 | |||||||
chr10:102317285 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.164-26766T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102317285 | |||||||
chr10:102317596 | C | T | 1 | a0001c0001t0001g0296 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.164-26455C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102317596 | |||||||
chr10:102317625 | A | G | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-26426A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102317625 | |||||||
chr10:102317711 | C | T | 1 | a0001c0001t0001g0011 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.164-26340C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102317711 | |||||||
chr10:102317746 | C | T | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-26305C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102317746 | |||||||
chr10:102317901 | T | TTTTTA | 94 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(91): Show |
95 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.164-26146_164-2614 others(9): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102317901 | ||||||
chr10:102317904 | T | A | 5 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-26147T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102317904 | |||||||
chr10:102317906 | A | T | 5 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 others(2): Show |
5 | HG01891.hp1 HG02109.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-26145A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102317906 | |||||||
chr10:102318118 | G | C | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-25933G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102318118 | |||||||
chr10:102318287 | A | G | 11 | a0002c0002t0001g0107 a0002c0002t0001g0171 a0002c0002t0001g0172 others(8): Show |
11 | HG00735.hp2 HG01099.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-25764A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102318287 | |||||||
chr10:102318475 | G | GC | 96 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(93): Show |
97 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.164-25575dupC | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102318475 | ||||||
chr10:102318535 | T | C | 1 | a0001c0003t0001g0226 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.164-25516T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102318535 | |||||||
chr10:102318677 | C | A | 5 | a0001c0001t0001g0119 a0001c0001t0001g0126 a0001c0001t0001g0127 others(2): Show |
5 | HG02280.hp2 HG02717.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-25374C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102318677 | |||||||
chr10:102318830 | G | A | 1 | a0001c0001t0005g0155 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.164-25221G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102318830 | |||||||
chr10:102318894 | C | G | 5 | a0001c0001t0001g0114 a0001c0001t0001g0118 a0001c0001t0001g0120 others(2): Show |
5 | HG01109.hp2 HG02451.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-25157C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102318894 | |||||||
chr10:102319003 | G | C | 96 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(93): Show |
97 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.164-25048G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102319003 | |||||||
chr10:102319151 | A | C | 24 | a0001c0001t0001g0208 a0001c0001t0001g0212 a0001c0001t0001g0213 others(21): Show |
24 | HG01070.hp2 HG01081.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.164-24900A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102319151 | |||||||
chr10:102319181 | G | A | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-24870G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102319181 | |||||||
chr10:102319245 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.164-24806G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102319245 | |||||||
chr10:102319261 | A | G | 1 | a0001c0001t0001g0106 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.164-24790A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102319261 | |||||||
chr10:102319277 | G | A | 3 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0038 |
3 | HG02523.hp2 NA19004.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.164-24774G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102319277 | |||||||
chr10:102319318 | TCAA | T | 56 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(53): Show |
56 | HG00544.hp1 HG00609.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.164-24717_164-2471 others(7): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102319318 | ||||||
chr10:102319334 | C | A | 94 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(91): Show |
95 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.164-24717C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102319334 | |||||||
chr10:102319374 | T | TA | 106 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0114 others(103): Show |
107 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.164-24668dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102319374 | ||||||
chr10:102319728 | C | CT | 15 | a0001c0001t0001g0106 a0001c0001t0001g0161 a0001c0001t0001g0162 others(12): Show |
15 | HG00544.hp1 HG00609.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.164-24306dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102319728 | ||||||
chr10:102319728 | CT | C | 13 | a0001c0001t0001g0011 a0001c0001t0001g0113 a0001c0001t0001g0133 others(10): Show |
13 | HG01169.hp1 HG01496.hp2 HG01515.hp2 others(10): Show |
intron_variant | MODIFIER | c.164-24306delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102319728 | ||||||
chr10:102319814 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.164-24237C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102319814 | |||||||
chr10:102320061 | T | C | 58 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(55): Show |
58 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.164-23990T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102320061 | |||||||
chr10:102320099 | A | T | 1 | a0001c0001t0001g0154 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.164-23952A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102320099 | |||||||
chr10:102320196 | A | G | 3 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 |
4 | HG02280.hp1 NA18522.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-23855A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102320196 | |||||||
chr10:102320275 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.164-23776T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102320275 | |||||||
chr10:102320368 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.164-23683G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102320368 | |||||||
chr10:102320471 | A | G | 28 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(25): Show |
28 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.164-23580A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102320471 | |||||||
chr10:102320560 | G | C | 2 | a0001c0001t0003g0279 a0001c0001t0003g0289 |
2 | HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.164-23491G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102320560 | |||||||
chr10:102320826 | C | T | 2 | a0001c0001t0001g0207 a0001c0001t0005g0155 |
2 | HG00280.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.164-23225C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102320826 | |||||||
chr10:102321011 | G | C | 2 | a0001c0001t0002g0083 a0001c0001t0002g0084 |
2 | HG00741.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.164-23040G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102321011 | |||||||
chr10:102321056 | G | A | 2 | a0001c0001t0001g0236 a0001c0001t0001g0251 |
2 | HG02258.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.164-22995G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102321056 | |||||||
chr10:102321085 | G | A | 9 | a0001c0001t0001g0153 a0001c0001t0001g0184 a0001c0001t0001g0189 others(6): Show |
9 | HG01928.hp1 HG01934.hp1 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-22966G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102321085 | |||||||
chr10:102321356 | ATCTT | A | 7 | a0002c0002t0001g0107 a0002c0002t0001g0177 a0002c0002t0001g0198 others(4): Show |
7 | HG00735.hp2 HG01123.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-22689_164-2268 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102321356 | ||||||
chr10:102321592 | C | T | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0013 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.164-22459C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102321592 | |||||||
chr10:102321624 | T | C | 3 | a0001c0001t0002g0013 a0001c0001t0002g0070 a0001c0001t0002g0071 |
3 | HG01346.hp1 HG01361.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.164-22427T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102321624 | |||||||
chr10:102321632 | C | T | 87 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0190 others(84): Show |
88 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(85): Show |
intron_variant | MODIFIER | c.164-22419C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102321632 | |||||||
chr10:102321759 | G | A | 6 | a0001c0003t0001g0206 a0001c0003t0001g0224 a0001c0003t0001g0226 others(3): Show |
6 | HG01081.hp1 HG02451.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-22292G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102321759 | |||||||
chr10:102321789 | T | G | 3 | a0004c0008t0001g0194 a0004c0008t0001g0199 a0004c0020t0003g0311 |
3 | NA18949.hp2 NA18957.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.164-22262T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102321789 | |||||||
chr10:102321879 | G | A | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-22172G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102321879 | |||||||
chr10:102322032 | G | T | 1 | a0001c0024t0001g0228 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.164-22019G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102322032 | |||||||
chr10:102322369 | A | G | 1 | a0001c0001t0001g0123 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.164-21682A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102322369 | |||||||
chr10:102322440 | T | C | 2 | a0001c0001t0002g0035 a0006c0015t0002g0061 |
2 | HG00738.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.164-21611T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102322440 | |||||||
chr10:102322545 | C | T | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-21506C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102322545 | |||||||
chr10:102322718 | CA | C | 173 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(170): Show |
174 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.164-21307delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102322718 | ||||||
chr10:102322718 | CAA | C | 94 | a0001c0001t0001g0012 a0001c0001t0001g0131 a0001c0001t0001g0132 others(91): Show |
94 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.164-21308_164-2130 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102322718 | ||||||
chr10:102322718 | CAAAAAAA | C | 21 | a0001c0001t0001g0208 a0001c0001t0001g0214 a0001c0001t0001g0215 others(18): Show |
21 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(18): Show |
intron_variant | MODIFIER | c.164-21313_164-2130 others(11): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102322718 | ||||||
chr10:102322882 | A | G | 2 | a0001c0001t0001g0323 a0001c0001t0001g0326 |
2 | HG03516.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.164-21169A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102322882 | |||||||
chr10:102322931 | T | G | 122 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(119): Show |
122 | HG00099.hp2 HG00280.hp2 HG00544.hp2 others(119): Show |
intron_variant | MODIFIER | c.164-21120T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102322931 | |||||||
chr10:102322934 | G | T | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-21117G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102322934 | |||||||
chr10:102323010 | G | A | 1 | a0001c0001t0001g0150 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.164-21041G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102323010 | |||||||
chr10:102323117 | A | C | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-20934A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102323117 | |||||||
chr10:102323121 | C | A | 1 | a0001c0003t0001g0226 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.164-20930C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102323121 | |||||||
chr10:102323167 | CT | C | 90 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.164-20880delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102323167 | ||||||
chr10:102323196 | G | A | 1 | a0001c0001t0005g0155 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.164-20855G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102323196 | |||||||
chr10:102323239 | G | GA | 16 | a0001c0001t0001g0154 a0001c0001t0001g0167 a0001c0001t0001g0190 others(13): Show |
16 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(13): Show |
intron_variant | MODIFIER | c.164-20790dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102323239 | ||||||
chr10:102323239 | G | GAA | 23 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(20): Show |
23 | HG00544.hp2 HG00621.hp1 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.164-20791_164-2079 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102323239 | ||||||
chr10:102323239 | GA | G | 10 | a0001c0001t0001g0182 a0001c0001t0002g0035 a0001c0003t0001g0209 others(7): Show |
11 | HG01070.hp2 HG01074.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.164-20790delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102323239 | ||||||
chr10:102323259 | A | G | 3 | a0001c0001t0002g0036 a0001c0001t0002g0045 a0001c0004t0002g0103 |
3 | HG01358.hp1 HG03942.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.164-20792A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102323259 | |||||||
chr10:102323388 | C | T | 2 | a0001c0001t0001g0154 a0007c0011t0001g0294 |
2 | HG01074.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.164-20663C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102323388 | |||||||
chr10:102323431 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.164-20620G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102323431 | |||||||
chr10:102323575 | CT | C | 9 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0323 others(6): Show |
9 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-20461delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102323575 | ||||||
chr10:102324151 | T | C | 28 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(25): Show |
28 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.164-19900T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102324151 | |||||||
chr10:102324193 | A | G | 1 | a0001c0001t0002g0028 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.164-19858A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102324193 | |||||||
chr10:102324269 | C | A | 1 | a0003c0005t0002g0077 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.164-19782C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102324269 | |||||||
chr10:102324371 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.164-19680A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102324371 | |||||||
chr10:102324411 | G | T | 1 | a0001c0001t0002g0047 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.164-19640G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102324411 | |||||||
chr10:102324610 | G | A | 1 | a0001c0001t0002g0072 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.164-19441G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102324610 | |||||||
chr10:102324700 | C | T | 1 | a0001c0001t0003g0282 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.164-19351C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102324700 | |||||||
chr10:102324978 | A | G | 5 | a0003c0005t0002g0060 a0003c0005t0002g0076 a0003c0005t0002g0077 others(2): Show |
5 | HG02071.hp1 NA18952.hp1 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-19073A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102324978 | |||||||
chr10:102325132 | A | G | 56 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(53): Show |
56 | HG00544.hp1 HG00609.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.164-18919A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102325132 | |||||||
chr10:102325148 | C | CTCCCCGA others(7): Show |
1 | a0001c0001t0001g0236 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.164-18898_164-1888 others(18): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102325148 | ||||||
chr10:102325154 | G | A | 5 | a0001c0001t0001g0189 a0001c0001t0001g0200 a0004c0008t0001g0194 others(2): Show |
5 | HG02074.hp2 NA18612.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-18897G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102325154 | |||||||
chr10:102325324 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.164-18727G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102325324 | |||||||
chr10:102325378 | C | T | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-18673C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102325378 | |||||||
chr10:102325550 | C | CA | 93 | a0001c0001t0001g0154 a0001c0001t0001g0319 a0001c0001t0001g0323 others(90): Show |
94 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(91): Show |
intron_variant | MODIFIER | c.164-18485dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102325550 | ||||||
chr10:102325550 | C | CAA | 10 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0017 others(7): Show |
10 | HG01109.hp1 HG01928.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.164-18486_164-1848 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102325550 | ||||||
chr10:102325550 | CA | C | 6 | a0001c0001t0001g0251 a0001c0001t0001g0292 a0001c0001t0001g0295 others(3): Show |
6 | HG00099.hp1 HG02895.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-18485delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102325550 | ||||||
chr10:102325610 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.164-18441G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102325610 | |||||||
chr10:102325726 | T | C | 31 | a0001c0001t0002g0004 a0001c0001t0002g0072 a0001c0001t0002g0073 others(28): Show |
31 | HG00558.hp1 HG00621.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.164-18325T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102325726 | |||||||
chr10:102325727 | G | T | 3 | a0001c0001t0002g0018 a0001c0001t0002g0065 a0001c0001t0002g0066 |
3 | HG01069.hp2 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.164-18324G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102325727 | |||||||
chr10:102326164 | C | T | 82 | a0001c0001t0001g0190 a0001c0001t0001g0230 a0001c0001t0001g0236 others(79): Show |
83 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.164-17887C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102326164 | |||||||
chr10:102326319 | T | C | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-17732T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102326319 | |||||||
chr10:102326323 | A | G | 4 | a0001c0001t0002g0017 a0001c0001t0002g0034 a0009c0019t0002g0042 others(1): Show |
4 | HG01928.hp2 HG02109.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-17728A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102326323 | |||||||
chr10:102327151 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.164-16900G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102327151 | |||||||
chr10:102327153 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.164-16898G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102327153 | |||||||
chr10:102327199 | G | A | 1 | a0001c0001t0001g0300 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.164-16852G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102327199 | |||||||
chr10:102327339 | A | G | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-16712A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102327339 | |||||||
chr10:102327457 | G | A | 5 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0022 others(2): Show |
5 | HG00099.hp2 HG01255.hp2 HG03017.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-16594G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102327457 | |||||||
chr10:102327472 | A | G | 19 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(16): Show |
19 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.164-16579A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102327472 | |||||||
chr10:102327560 | C | T | 1 | a0001c0001t0001g0300 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.164-16491C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102327560 | |||||||
chr10:102327599 | T | C | 320 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(317): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.164-16452T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102327599 | |||||||
chr10:102327959 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.164-16092C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102327959 | |||||||
chr10:102328107 | G | A | 28 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(25): Show |
28 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.164-15944G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102328107 | |||||||
chr10:102328174 | T | G | 1 | a0001c0001t0001g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.164-15877T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102328174 | |||||||
chr10:102328340 | A | T | 1 | a0001c0001t0002g0013 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.164-15711A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102328340 | |||||||
chr10:102328373 | G | A | 1 | a0001c0001t0003g0264 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.164-15678G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102328373 | |||||||
chr10:102328543 | A | G | 2 | a0001c0001t0001g0006 a0001c0001t0001g0151 |
2 | HG01175.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.164-15508A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102328543 | |||||||
chr10:102328545 | G | A | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-15506G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102328545 | |||||||
chr10:102329184 | C | T | 1 | a0002c0002t0001g0205 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.164-14867C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102329184 | |||||||
chr10:102329269 | C | T | 9 | a0001c0001t0001g0105 a0001c0001t0001g0158 a0001c0001t0001g0159 others(6): Show |
9 | HG02293.hp2 NA18954.hp1 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-14782C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102329269 | |||||||
chr10:102329357 | T | A | 4 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(1): Show |
4 | HG02717.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-14694T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102329357 | |||||||
chr10:102329554 | C | G | 1 | a0001c0001t0002g0051 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.164-14497C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102329554 | |||||||
chr10:102329658 | T | G | 112 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0109 others(109): Show |
113 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(110): Show |
intron_variant | MODIFIER | c.164-14393T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102329658 | |||||||
chr10:102329664 | C | T | 112 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0109 others(109): Show |
113 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(110): Show |
intron_variant | MODIFIER | c.164-14387C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102329664 | |||||||
chr10:102330512 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.164-13539C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102330512 | |||||||
chr10:102330554 | C | T | 7 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(4): Show |
7 | HG01106.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.164-13497C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102330554 | |||||||
chr10:102330555 | A | G | 320 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(317): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.164-13496A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102330555 | |||||||
chr10:102330579 | A | G | 18 | a0001c0001t0001g0114 a0001c0001t0001g0115 a0001c0001t0001g0116 others(15): Show |
18 | HG01109.hp2 HG01891.hp2 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.164-13472A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102330579 | |||||||
chr10:102330596 | G | T | 1 | a0001c0001t0001g0240 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.164-13455G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102330596 | |||||||
chr10:102330686 | C | CA | 8 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(5): Show |
9 | HG01516.hp1 HG01517.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.164-13355dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102330686 | ||||||
chr10:102330693 | A | T | 1 | a0001c0001t0002g0082 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.164-13358A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102330693 | |||||||
chr10:102330788 | G | C | 1 | a0001c0001t0002g0050 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.164-13263G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102330788 | |||||||
chr10:102331065 | G | T | 1 | a0008c0018t0001g0204 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.164-12986G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102331065 | |||||||
chr10:102331161 | G | A | 10 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0017 others(7): Show |
10 | HG01109.hp1 HG01928.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.164-12890G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102331161 | |||||||
chr10:102331328 | C | T | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-12723C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102331328 | |||||||
chr10:102331339 | A | T | 1 | a0001c0001t0005g0155 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.164-12712A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102331339 | |||||||
chr10:102331851 | A | AT | 46 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0118 others(43): Show |
46 | HG00280.hp1 HG00558.hp1 HG00642.hp2 others(43): Show |
intron_variant | MODIFIER | c.164-12174dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102331851 | ||||||
chr10:102331851 | A | ATT | 33 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0004 others(30): Show |
33 | HG00621.hp2 HG01069.hp1 HG01069.hp2 others(30): Show |
intron_variant | MODIFIER | c.164-12175_164-1217 others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102331851 | ||||||
chr10:102331851 | A | ATTT | 36 | a0001c0001t0002g0013 a0001c0001t0002g0019 a0001c0001t0002g0020 others(33): Show |
36 | HG00099.hp2 HG00280.hp2 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.164-12176_164-1217 others(7): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102331851 | ||||||
chr10:102331851 | A | ATTTT | 9 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0035 others(6): Show |
9 | HG00673.hp1 HG00738.hp1 HG01074.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-12177_164-1217 others(8): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102331851 | ||||||
chr10:102331851 | A | ATTTTT | 8 | a0001c0001t0002g0026 a0001c0001t0002g0052 a0001c0001t0002g0053 others(5): Show |
8 | NA18955.hp1 NA18959.hp1 NA18968.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-12178_164-1217 others(9): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102331851 | ||||||
chr10:102331851 | A | ATTTTTTT others(13): Show |
2 | a0001c0004t0004g0001 a0001c0004t0004g0016 |
3 | HG02280.hp1 HG02965.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.164-12193_164-1217 others(24): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102331851 | ||||||
chr10:102331851 | A | ATTTTTTT others(14): Show |
2 | a0001c0004t0004g0005 a0001c0004t0004g0014 |
2 | NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.164-12194_164-1217 others(25): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102331851 | ||||||
chr10:102331851 | AT | A | 22 | a0001c0001t0001g0109 a0001c0001t0001g0111 a0001c0001t0001g0154 others(19): Show |
22 | HG01070.hp2 HG01074.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.164-12174delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102331851 | ||||||
chr10:102331925 | T | C | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-12126T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102331925 | |||||||
chr10:102332080 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.164-11971G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102332080 | |||||||
chr10:102332139 | T | C | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-11912T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102332139 | |||||||
chr10:102332235 | C | T | 3 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0038 |
3 | HG02523.hp2 NA19004.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.164-11816C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102332235 | |||||||
chr10:102332279 | C | T | 5 | a0001c0001t0001g0230 a0001c0001t0001g0251 a0001c0001t0001g0252 others(2): Show |
5 | HG02922.hp1 HG03041.hp2 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.164-11772C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102332279 | |||||||
chr10:102332387 | C | CT | 88 | a0001c0001t0001g0141 a0001c0001t0001g0185 a0001c0001t0001g0212 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.164-11651dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102332387 | ||||||
chr10:102332487 | G | A | 1 | a0001c0001t0003g0235 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.164-11564G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102332487 | |||||||
chr10:102333110 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.164-10941G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102333110 | |||||||
chr10:102333196 | A | G | 3 | a0002c0002t0001g0171 a0002c0002t0001g0181 a0002c0002t0001g0187 |
3 | HG01099.hp1 HG01361.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.164-10855A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102333196 | |||||||
chr10:102333331 | A | G | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-10720A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102333331 | |||||||
chr10:102333885 | T | G | 2 | a0003c0005t0002g0060 a0003c0005t0002g0101 |
2 | HG02071.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.164-10166T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102333885 | |||||||
chr10:102333901 | C | A | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-10150C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102333901 | |||||||
chr10:102334176 | A | G | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-9875A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102334176 | |||||||
chr10:102334367 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.164-9684A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102334367 | |||||||
chr10:102334722 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.164-9329G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102334722 | |||||||
chr10:102334741 | C | T | 22 | a0001c0001t0001g0208 a0001c0001t0001g0214 a0001c0001t0001g0215 others(19): Show |
22 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.164-9310C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102334741 | |||||||
chr10:102334773 | G | A | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-9278G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102334773 | |||||||
chr10:102334848 | CA | C | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-9187delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102334848 | ||||||
chr10:102334861 | A | G | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-9190A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102334861 | |||||||
chr10:102334881 | A | G | 1 | a0001c0001t0003g0312 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.164-9170A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102334881 | |||||||
chr10:102334971 | C | G | 6 | a0001c0001t0002g0090 a0001c0001t0002g0091 a0001c0001t0002g0092 others(3): Show |
6 | NA18953.hp1 NA18967.hp2 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-9080C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102334971 | |||||||
chr10:102335200 | A | G | 1 | a0002c0002t0001g0172 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.164-8851A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102335200 | |||||||
chr10:102335244 | TGACTGGC others(15): Show |
T | 4 | a0001c0001t0003g0283 a0001c0001t0003g0284 a0001c0001t0003g0285 others(1): Show |
4 | NA18950.hp2 NA18979.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-8803_164-8782d others(24): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102335244 | ||||||
chr10:102335289 | T | C | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-8762T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102335289 | |||||||
chr10:102335383 | G | A | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-8668G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102335383 | |||||||
chr10:102335773 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.164-8278C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102335773 | |||||||
chr10:102335891 | A | G | 1 | a0001c0001t0002g0024 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.164-8160A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102335891 | |||||||
chr10:102335986 | A | G | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-8065A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102335986 | |||||||
chr10:102336043 | T | C | 1 | a0001c0001t0003g0257 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.164-8008T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102336043 | |||||||
chr10:102336054 | C | G | 31 | a0001c0001t0002g0004 a0001c0001t0002g0072 a0001c0001t0002g0073 others(28): Show |
31 | HG00558.hp1 HG00621.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.164-7997C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102336054 | |||||||
chr10:102336199 | G | A | 5 | a0001c0003t0001g0108 a0001c0003t0001g0209 a0001c0003t0001g0210 others(2): Show |
5 | HG01070.hp2 HG01516.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-7852G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102336199 | |||||||
chr10:102336226 | G | C | 1 | a0001c0001t0003g0275 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.164-7825G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102336226 | |||||||
chr10:102336299 | CA | C | 6 | a0001c0001t0002g0046 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-7737delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102336299 | ||||||
chr10:102336302 | AAAAAAAA others(6): Show |
A | 13 | a0001c0001t0001g0106 a0001c0001t0001g0185 a0001c0001t0001g0208 others(10): Show |
13 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.164-7732_164-7720d others(15): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102336302 | ||||||
chr10:102336316 | A | G | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-7735A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102336316 | |||||||
chr10:102336839 | A | ATGAT | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-7212_164-7211i others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102336839 | |||||||
chr10:102336975 | A | T | 59 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(56): Show |
59 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(56): Show |
intron_variant | MODIFIER | c.164-7076A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102336975 | |||||||
chr10:102337104 | C | T | 1 | a0001c0001t0002g0019 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.164-6947C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337104 | |||||||
chr10:102337165 | T | G | 1 | a0001c0001t0001g0134 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.164-6886T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337165 | |||||||
chr10:102337295 | G | GCGAACCC others(1): Show |
325 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(322): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.164-6754_164-6753i others(10): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102337295 | ||||||
chr10:102337298 | T | A | 325 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(322): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.164-6753T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337298 | |||||||
chr10:102337301 | G | C | 325 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(322): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.164-6750G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337301 | |||||||
chr10:102337369 | C | CA | 165 | a0001c0001t0001g0109 a0001c0001t0001g0119 a0001c0001t0001g0128 others(162): Show |
166 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.164-6665dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102337369 | ||||||
chr10:102337369 | C | CAA | 10 | a0001c0001t0001g0212 a0001c0001t0001g0246 a0001c0001t0002g0054 others(7): Show |
10 | HG00609.hp1 HG01109.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.164-6666_164-6665d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102337369 | ||||||
chr10:102337381 | A | C | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-6670A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337381 | |||||||
chr10:102337501 | A | G | 1 | a0001c0001t0002g0050 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.164-6550A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337501 | |||||||
chr10:102337604 | C | A | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-6447C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337604 | |||||||
chr10:102337615 | G | C | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-6436G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337615 | |||||||
chr10:102337806 | G | A | 1 | a0001c0001t0002g0035 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.164-6245G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337806 | |||||||
chr10:102337858 | AAAAG | A | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.164-6173_164-6170d others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102337858 | ||||||
chr10:102337961 | T | C | 1 | a0001c0001t0002g0063 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.164-6090T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337961 | |||||||
chr10:102337977 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.164-6074C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102337977 | |||||||
chr10:102338237 | C | CT | 47 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(44): Show |
47 | HG00544.hp2 HG00621.hp1 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.164-5793dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102338237 | ||||||
chr10:102338237 | C | CTTTT | 9 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0001g0120 others(6): Show |
9 | HG01109.hp2 HG01891.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.164-5796_164-5793d others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102338237 | ||||||
chr10:102338237 | C | CTTTTT | 9 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(6): Show |
9 | HG01891.hp2 HG02145.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.164-5797_164-5793d others(7): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102338237 | ||||||
chr10:102338239 | T | TC | 5 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-5812_164-5811i others(3): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102338239 | |||||||
chr10:102338240 | T | C | 1 | a0001c0004t0004g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.164-5811T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102338240 | |||||||
chr10:102338407 | A | T | 5 | a0001c0001t0002g0024 a0001c0001t0002g0035 a0001c0001t0002g0063 others(2): Show |
5 | HG00738.hp1 HG01074.hp2 HG01099.hp2 others(2): Show |
intron_variant | MODIFIER | c.164-5644A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102338407 | |||||||
chr10:102338470 | G | C | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-5581G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102338470 | |||||||
chr10:102338554 | A | G | 2 | a0001c0004t0004g0005 a0001c0004t0004g0014 |
2 | NA19030.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.164-5497A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102338554 | |||||||
chr10:102338932 | A | G | 11 | a0001c0001t0001g0208 a0001c0001t0001g0214 a0001c0001t0001g0215 others(8): Show |
11 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.164-5119A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102338932 | |||||||
chr10:102339085 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0297 others(1): Show |
4 | HG02559.hp1 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-4966G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102339085 | |||||||
chr10:102339129 | G | A | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-4922G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102339129 | |||||||
chr10:102339192 | G | A | 90 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.164-4859G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102339192 | |||||||
chr10:102339425 | G | A | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-4626G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102339425 | |||||||
chr10:102339470 | T | C | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-4581T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102339470 | |||||||
chr10:102339530 | G | A | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.164-4521G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102339530 | |||||||
chr10:102339552 | A | G | 1 | a0001c0001t0007g0146 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.164-4499A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102339552 | |||||||
chr10:102339695 | A | G | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | NA19002.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.164-4356A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102339695 | |||||||
chr10:102339700 | T | C | 1 | a0001c0001t0002g0045 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.164-4351T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102339700 | |||||||
chr10:102339953 | A | AT | 222 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(219): Show |
223 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(220): Show |
intron_variant | MODIFIER | c.164-4080dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102339953 | ||||||
chr10:102339953 | A | ATT | 22 | a0001c0001t0001g0011 a0001c0001t0001g0114 a0001c0001t0001g0118 others(19): Show |
22 | HG00609.hp1 HG01109.hp2 HG01516.hp1 others(19): Show |
intron_variant | MODIFIER | c.164-4081_164-4080d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102339953 | ||||||
chr10:102340060 | T | C | 1 | a0001c0001t0003g0250 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.164-3991T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102340060 | |||||||
chr10:102340101 | G | A | 3 | a0001c0001t0003g0002 a0001c0001t0003g0272 a0001c0001t0003g0278 |
4 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.164-3950G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102340101 | |||||||
chr10:102340263 | A | G | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164-3788A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102340263 | |||||||
chr10:102340267 | C | CT | 92 | a0001c0001t0001g0011 a0001c0001t0001g0109 a0001c0001t0001g0116 others(89): Show |
92 | HG00544.hp2 HG00558.hp2 HG00673.hp2 others(89): Show |
intron_variant | MODIFIER | c.164-3761dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102340267 | ||||||
chr10:102340267 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.164-3784C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102340267 | |||||||
chr10:102340352 | A | C | 23 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0214 others(20): Show |
23 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.164-3699A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102340352 | |||||||
chr10:102340482 | C | T | 3 | a0001c0001t0003g0231 a0001c0001t0003g0232 a0001c0001t0003g0233 |
3 | HG00609.hp1 NA18959.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.164-3569C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102340482 | |||||||
chr10:102340878 | G | A | 1 | a0002c0002t0001g0172 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.164-3173G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102340878 | |||||||
chr10:102340976 | G | A | 4 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0138 others(1): Show |
4 | HG00642.hp1 HG00738.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.164-3075G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102340976 | |||||||
chr10:102341056 | T | C | 6 | a0001c0001t0002g0018 a0001c0001t0002g0051 a0001c0001t0002g0058 others(3): Show |
6 | HG00280.hp2 HG01069.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.164-2995T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102341056 | |||||||
chr10:102341264 | A | G | 1 | a0001c0001t0003g0241 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.164-2787A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102341264 | |||||||
chr10:102341382 | G | A | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-2669G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102341382 | |||||||
chr10:102341658 | A | G | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-2393A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102341658 | |||||||
chr10:102341800 | A | C | 1 | a0001c0001t0001g0195 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.164-2251A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102341800 | |||||||
chr10:102341899 | C | T | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-2152C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102341899 | |||||||
chr10:102341900 | G | T | 1 | a0001c0001t0002g0031 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.164-2151G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102341900 | |||||||
chr10:102341903 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.164-2148T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102341903 | |||||||
chr10:102341927 | C | A | 1 | a0001c0001t0001g0327 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.164-2124C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102341927 | |||||||
chr10:102342038 | C | CT | 28 | a0001c0001t0001g0189 a0001c0001t0001g0207 a0001c0001t0001g0208 others(25): Show |
28 | HG01070.hp2 HG01074.hp1 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.164-1997dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102342038 | ||||||
chr10:102342259 | G | C | 1 | a0001c0001t0001g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.164-1792G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102342259 | |||||||
chr10:102342361 | G | A | 57 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(54): Show |
57 | HG00544.hp1 HG00609.hp2 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.164-1690G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102342361 | |||||||
chr10:102342387 | ACG | A | 11 | a0001c0001t0001g0208 a0001c0001t0001g0214 a0001c0001t0001g0215 others(8): Show |
11 | HG02145.hp1 HG02257.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.164-1662_164-1661d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102342387 | ||||||
chr10:102342389 | G | GCA | 17 | a0001c0001t0001g0207 a0001c0003t0001g0108 a0001c0003t0001g0206 others(14): Show |
18 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.164-1644_164-1643d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102342389 | ||||||
chr10:102342389 | GCA | G | 3 | a0001c0001t0001g0148 a0001c0001t0001g0254 a0001c0001t0002g0029 |
3 | HG02258.hp2 HG03516.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.164-1644_164-1643d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102342389 | ||||||
chr10:102342574 | G | A | 96 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(93): Show |
97 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.164-1477G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102342574 | |||||||
chr10:102342746 | T | G | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.164-1305T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102342746 | |||||||
chr10:102342854 | A | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0167 a0001c0001t0001g0180 others(5): Show |
8 | HG02040.hp2 HG02683.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.164-1197A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102342854 | |||||||
chr10:102343547 | G | C | 2 | a0001c0001t0001g0293 a0001c0001t0001g0319 |
2 | NA18963.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.164-504G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102343547 | |||||||
chr10:102343588 | C | T | 2 | a0001c0001t0002g0018 a0001c0001t0002g0065 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.164-463C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102343588 | |||||||
chr10:102343597 | T | C | 1 | a0001c0001t0003g0261 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.164-454T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | chr10 | 102343597 | |||||||
chr10:102343799 | C | CA | 21 | a0001c0001t0001g0179 a0001c0001t0001g0185 a0001c0001t0001g0295 others(18): Show |
21 | HG00735.hp2 HG01099.hp1 HG01123.hp1 others(18): Show |
intron_variant | MODIFIER | c.164-235dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102343799 | ||||||
chr10:102343799 | CA | C | 224 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0109 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(223): Show |
intron_variant | MODIFIER | c.164-235delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 3/39 | INFO_REALIGN_3_PRIME | chr10 | 102343799 | ||||||
chr10:102344465 | G | GGTTT | 102 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0109 others(99): Show |
103 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.295+308_295+311dup others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102344465 | ||||||
chr10:102344601 | C | T | 1 | a0001c0001t0003g0302 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.295+419C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102344601 | |||||||
chr10:102344680 | C | T | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.295+498C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102344680 | |||||||
chr10:102344812 | A | G | 325 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(322): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.295+630A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102344812 | |||||||
chr10:102344908 | T | C | 2 | a0001c0001t0003g0279 a0001c0001t0003g0289 |
2 | HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.295+726T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102344908 | |||||||
chr10:102344940 | G | T | 2 | a0001c0003t0001g0226 a0001c0003t0001g0227 |
2 | HG02451.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.295+758G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102344940 | |||||||
chr10:102345065 | C | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0138 |
2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.295+883C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102345065 | |||||||
chr10:102345066 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.295+884G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102345066 | |||||||
chr10:102345112 | T | C | 16 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0131 others(13): Show |
16 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.295+930T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102345112 | |||||||
chr10:102345281 | C | CA | 8 | a0001c0001t0001g0321 a0001c0001t0003g0289 a0001c0003t0001g0221 others(5): Show |
9 | HG02280.hp1 HG02738.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.295+1115dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102345281 | ||||||
chr10:102345281 | CA | C | 90 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.295+1115delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102345281 | ||||||
chr10:102345424 | G | A | 1 | a0001c0003t0001g0322 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.295+1242G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102345424 | |||||||
chr10:102345639 | TC | T | 30 | a0001c0001t0002g0004 a0001c0001t0002g0072 a0001c0001t0002g0073 others(27): Show |
30 | HG00558.hp1 HG00621.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.295+1459delC | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102345639 | ||||||
chr10:102345642 | G | A | 5 | a0001c0001t0001g0114 a0001c0001t0001g0118 a0001c0001t0001g0120 others(2): Show |
5 | HG01109.hp2 HG02451.hp1 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.295+1460G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102345642 | |||||||
chr10:102345646 | C | CA | 70 | a0001c0001t0001g0006 a0001c0001t0001g0111 a0001c0001t0001g0114 others(67): Show |
70 | HG00544.hp1 HG00544.hp2 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.295+1490dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102345646 | ||||||
chr10:102345646 | CA | C | 14 | a0001c0001t0001g0011 a0001c0001t0001g0133 a0001c0001t0001g0135 others(11): Show |
14 | HG01496.hp2 HG01515.hp2 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.295+1490delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102345646 | ||||||
chr10:102345646 | CAAAA | C | 8 | a0001c0001t0002g0026 a0001c0001t0002g0053 a0001c0004t0002g0103 others(5): Show |
9 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.295+1487_295+1490d others(6): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102345646 | ||||||
chr10:102345646 | CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0001g0293 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.295+1478_295+1490d others(15): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102345646 | ||||||
chr10:102345794 | T | C | 6 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0145 others(3): Show |
6 | HG00558.hp2 HG01978.hp1 NA18963.hp2 others(3): Show |
intron_variant | MODIFIER | c.295+1612T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102345794 | |||||||
chr10:102345822 | G | C | 1 | a0001c0004t0004g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.295+1640G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102345822 | |||||||
chr10:102345968 | G | C | 3 | a0001c0001t0001g0113 a0001c0001t0001g0135 a0001c0001t0001g0137 |
3 | HG01496.hp2 HG01515.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.295+1786G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102345968 | |||||||
chr10:102346085 | TTTTTTTA | T | 56 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(53): Show |
56 | HG00544.hp1 HG00609.hp2 HG00735.hp2 others(53): Show |
intron_variant | MODIFIER | c.295+1904_295+1910d others(9): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102346085 | |||||||
chr10:102346113 | C | T | 1 | a0001c0001t0003g0283 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.295+1931C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102346113 | |||||||
chr10:102346323 | T | G | 1 | a0001c0004t0004g0016 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.295+2141T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102346323 | |||||||
chr10:102346443 | T | C | 120 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0212 others(117): Show |
121 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.295+2261T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102346443 | |||||||
chr10:102346545 | G | T | 2 | a0001c0001t0001g0300 a0001c0001t0001g0301 |
2 | HG02622.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.295+2363G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102346545 | |||||||
chr10:102346577 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.295+2395C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102346577 | |||||||
chr10:102346601 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.295+2419G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102346601 | |||||||
chr10:102347434 | C | T | 2 | a0001c0001t0005g0152 a0001c0001t0005g0155 |
2 | HG00280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.295+3252C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102347434 | |||||||
chr10:102347497 | T | C | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.295+3315T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102347497 | |||||||
chr10:102347983 | T | C | 5 | a0001c0003t0001g0108 a0001c0003t0001g0209 a0001c0003t0001g0210 others(2): Show |
5 | HG01070.hp2 HG01516.hp2 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.296-3273T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102347983 | |||||||
chr10:102347990 | G | A | 1 | a0001c0001t0002g0017 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.296-3266G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102347990 | |||||||
chr10:102348571 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.296-2685G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102348571 | |||||||
chr10:102348657 | G | A | 3 | a0001c0001t0003g0002 a0001c0001t0003g0272 a0001c0001t0003g0278 |
4 | HG01070.hp1 HG01071.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.296-2599G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102348657 | |||||||
chr10:102349118 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.296-2138C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102349118 | |||||||
chr10:102349179 | T | A | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.296-2077T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102349179 | |||||||
chr10:102349349 | A | G | 113 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0109 others(110): Show |
114 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(111): Show |
intron_variant | MODIFIER | c.296-1907A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102349349 | |||||||
chr10:102349482 | A | T | 1 | a0001c0007t0001g0328 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.296-1774A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102349482 | |||||||
chr10:102349813 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.296-1443A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102349813 | |||||||
chr10:102350250 | T | C | 1 | a0001c0001t0001g0296 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.296-1006T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102350250 | |||||||
chr10:102350350 | C | CA | 6 | a0001c0001t0001g0185 a0001c0001t0001g0223 a0001c0001t0003g0273 others(3): Show |
6 | HG01123.hp1 HG02145.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-891dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102350350 | ||||||
chr10:102350350 | CA | C | 6 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(3): Show |
7 | HG01081.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.296-891delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102350350 | ||||||
chr10:102350395 | G | A | 1 | a0002c0002t0001g0203 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.296-861G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102350395 | |||||||
chr10:102350648 | T | G | 3 | a0001c0001t0002g0026 a0001c0001t0002g0053 a0001c0001t0002g0068 |
3 | NA18959.hp1 NA18980.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.296-608T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102350648 | |||||||
chr10:102350738 | A | C | 1 | a0001c0001t0002g0028 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.296-518A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102350738 | |||||||
chr10:102350849 | C | T | 1 | a0001c0001t0002g0082 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.296-407C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102350849 | |||||||
chr10:102350959 | C | T | 1 | a0001c0001t0002g0080 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.296-297C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102350959 | |||||||
chr10:102350977 | C | G | 1 | a0001c0001t0003g0260 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.296-279C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102350977 | |||||||
chr10:102350981 | G | A | 1 | a0001c0001t0001g0109 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.296-275G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | chr10 | 102350981 | |||||||
chr10:102351086 | C | CA | 35 | a0001c0001t0001g0006 a0001c0001t0001g0207 a0001c0001t0001g0214 others(32): Show |
35 | HG01070.hp2 HG01081.hp1 HG01123.hp1 others(32): Show |
intron_variant | MODIFIER | c.296-152dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102351086 | ||||||
chr10:102351086 | C | CAAAA | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.296-155_296-152dup others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 4/39 | INFO_REALIGN_3_PRIME | chr10 | 102351086 | ||||||
chr10:102351592 | TTAAA | T | 3 | a0001c0001t0001g0113 a0001c0001t0001g0135 a0001c0001t0001g0137 |
3 | HG01496.hp2 HG01515.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.414+221_414+224del others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 5/39 | INFO_REALIGN_3_PRIME | chr10 | 102351592 | ||||||
chr10:102351776 | T | G | 1 | a0001c0001t0001g0154 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.415-67T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 5/39 | chr10 | 102351776 | |||||||
chr10:102351783 | T | TACC | 31 | a0001c0001t0002g0004 a0001c0001t0002g0072 a0001c0001t0002g0073 others(28): Show |
31 | HG00558.hp1 HG00621.hp2 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.415-59_415-57dupAC others(1): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 5/39 | INFO_REALIGN_3_PRIME | chr10 | 102351783 | ||||||
chr10:102351813 | A | G | 12 | a0001c0001t0001g0106 a0001c0001t0001g0161 a0001c0001t0001g0162 others(9): Show |
12 | HG00544.hp1 HG00609.hp2 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.415-30A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 5/39 | chr10 | 102351813 | |||||||
chr10:102352054 | C | T | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.523+103C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 6/39 | chr10 | 102352054 | |||||||
chr10:102352077 | T | C | 2 | a0001c0001t0002g0036 a0001c0001t0002g0045 |
2 | HG01358.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.523+126T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 6/39 | chr10 | 102352077 | |||||||
chr10:102352137 | C | T | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.523+186C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 6/39 | chr10 | 102352137 | |||||||
chr10:102352232 | C | A | 2 | a0001c0001t0003g0313 a0001c0001t0003g0316 |
2 | HG02148.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.524-226C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 6/39 | chr10 | 102352232 | |||||||
chr10:102352246 | A | G | 2 | a0001c0001t0003g0279 a0001c0001t0003g0289 |
2 | HG03831.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.524-212A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 6/39 | chr10 | 102352246 | |||||||
chr10:102352451 | T | C | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.524-7T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 6/39 | chr10 | 102352451 | |||||||
chr10:102352570 | G | C | 1 | a0001c0001t0002g0047 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.584+52G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 7/39 | chr10 | 102352570 | |||||||
chr10:102352980 | T | C | 96 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(93): Show |
97 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.584+462T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 7/39 | chr10 | 102352980 | |||||||
chr10:102353059 | A | G | 23 | a0001c0001t0001g0207 a0001c0001t0001g0208 a0001c0001t0001g0214 others(20): Show |
23 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(20): Show |
intron_variant | MODIFIER | c.584+541A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 7/39 | chr10 | 102353059 | |||||||
chr10:102353184 | G | A | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.585-416G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 7/39 | chr10 | 102353184 | |||||||
chr10:102353213 | A | T | 2 | a0001c0001t0001g0115 a0001c0001t0001g0116 |
2 | HG02145.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.585-387A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 7/39 | chr10 | 102353213 | |||||||
chr10:102353784 | C | T | 4 | a0001c0001t0002g0091 a0001c0001t0002g0092 a0001c0001t0002g0093 others(1): Show |
4 | NA18967.hp2 NA18977.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.639+130C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102353784 | |||||||
chr10:102353944 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.639+290A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102353944 | |||||||
chr10:102354179 | C | T | 1 | a0001c0001t0002g0004 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.639+525C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102354179 | |||||||
chr10:102354275 | C | T | 2 | a0001c0001t0001g0182 a0001c0001t0003g0273 |
2 | NA18974.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.639+621C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102354275 | |||||||
chr10:102354473 | C | T | 1 | a0001c0001t0002g0074 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.639+819C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102354473 | |||||||
chr10:102354478 | CCT | C | 7 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0117 others(4): Show |
7 | HG01891.hp2 HG02145.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.639+829_639+830del others(2): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | INFO_REALIGN_3_PRIME | chr10 | 102354478 | ||||||
chr10:102354571 | T | C | 96 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(93): Show |
97 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.639+917T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102354571 | |||||||
chr10:102354715 | G | A | 4 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 others(1): Show |
4 | HG02717.hp1 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.639+1061G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102354715 | |||||||
chr10:102354729 | T | C | 1 | a0001c0003t0001g0224 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.639+1075T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102354729 | |||||||
chr10:102354767 | C | T | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.639+1113C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102354767 | |||||||
chr10:102354855 | T | A | 1 | a0001c0001t0002g0013 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.639+1201T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102354855 | |||||||
chr10:102354856 | C | A | 1 | a0001c0001t0002g0013 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.639+1202C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102354856 | |||||||
chr10:102354913 | CT | C | 118 | a0001c0001t0001g0106 a0001c0001t0001g0120 a0001c0001t0001g0142 others(115): Show |
119 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(116): Show |
intron_variant | MODIFIER | c.639+1277delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | INFO_REALIGN_3_PRIME | chr10 | 102354913 | ||||||
chr10:102355129 | C | T | 122 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0109 others(119): Show |
123 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(120): Show |
intron_variant | MODIFIER | c.639+1475C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102355129 | |||||||
chr10:102355277 | C | T | 5 | a0001c0001t0002g0021 a0001c0001t0002g0052 a0001c0001t0002g0054 others(2): Show |
5 | NA18951.hp1 NA18968.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.639+1623C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102355277 | |||||||
chr10:102355409 | T | C | 1 | a0001c0001t0001g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.639+1755T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102355409 | |||||||
chr10:102355505 | G | A | 2 | a0002c0002t0001g0177 a0002c0002t0001g0198 |
2 | HG01258.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.639+1851G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102355505 | |||||||
chr10:102355638 | A | T | 59 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(56): Show |
59 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.639+1984A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102355638 | |||||||
chr10:102355687 | A | T | 1 | a0001c0001t0001g0133 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.639+2033A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102355687 | |||||||
chr10:102356122 | G | A | 4 | a0001c0001t0003g0283 a0001c0001t0003g0284 a0001c0001t0003g0285 others(1): Show |
4 | NA18950.hp2 NA18979.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.640-1917G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102356122 | |||||||
chr10:102356138 | G | A | 3 | a0001c0001t0002g0018 a0001c0001t0002g0065 a0001c0001t0002g0066 |
3 | HG01069.hp2 HG01071.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.640-1901G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102356138 | |||||||
chr10:102356314 | C | T | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.640-1725C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102356314 | |||||||
chr10:102356562 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.640-1477G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102356562 | |||||||
chr10:102356692 | A | G | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.640-1347A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102356692 | |||||||
chr10:102356723 | C | T | 9 | a0001c0001t0001g0105 a0001c0001t0001g0158 a0001c0001t0001g0159 others(6): Show |
9 | HG02293.hp2 NA18954.hp1 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.640-1316C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102356723 | |||||||
chr10:102356766 | C | CA | 43 | a0001c0001t0001g0117 a0001c0001t0001g0123 a0001c0001t0001g0124 others(40): Show |
44 | HG00099.hp1 HG00642.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.640-1253dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | INFO_REALIGN_3_PRIME | chr10 | 102356766 | ||||||
chr10:102356766 | CA | C | 51 | a0001c0001t0001g0008 a0001c0001t0001g0154 a0001c0001t0001g0167 others(48): Show |
51 | HG00558.hp1 HG00621.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.640-1253delA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | INFO_REALIGN_3_PRIME | chr10 | 102356766 | ||||||
chr10:102356766 | CAA | C | 32 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0153 others(29): Show |
32 | HG00609.hp2 HG01928.hp1 HG01934.hp1 others(29): Show |
intron_variant | MODIFIER | c.640-1254_640-1253d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | INFO_REALIGN_3_PRIME | chr10 | 102356766 | ||||||
chr10:102357042 | A | G | 1 | a0001c0001t0001g0296 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.640-997A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102357042 | |||||||
chr10:102357252 | T | C | 96 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(93): Show |
97 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(94): Show |
intron_variant | MODIFIER | c.640-787T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102357252 | |||||||
chr10:102357486 | C | CA | 6 | a0001c0001t0001g0323 a0001c0001t0001g0324 a0001c0001t0001g0325 others(3): Show |
6 | HG01891.hp1 HG02109.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.640-536dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | INFO_REALIGN_3_PRIME | chr10 | 102357486 | ||||||
chr10:102357647 | T | C | 28 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0012 others(25): Show |
28 | HG00544.hp2 HG00558.hp2 HG00621.hp1 others(25): Show |
intron_variant | MODIFIER | c.640-392T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102357647 | |||||||
chr10:102357685 | C | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0145 |
2 | HG00558.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.640-354C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102357685 | |||||||
chr10:102357716 | T | C | 2 | a0001c0001t0003g0231 a0001c0001t0003g0233 |
2 | HG00609.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.640-323T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102357716 | |||||||
chr10:102357921 | T | A | 3 | a0002c0002t0001g0171 a0002c0002t0001g0181 a0002c0002t0001g0187 |
3 | HG01099.hp1 HG01361.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.640-118T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 8/39 | chr10 | 102357921 | |||||||
chr10:102358438 | C | T | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.788-68C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 9/39 | chr10 | 102358438 | |||||||
chr10:102358877 | T | C | 2 | a0001c0001t0005g0152 a0001c0001t0005g0155 |
2 | HG00280.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1011+148T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 10/39 | chr10 | 102358877 | |||||||
chr10:102359128 | G | A | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1012-139G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 10/39 | chr10 | 102359128 | |||||||
chr10:102359226 | G | C | 3 | a0002c0002t0001g0171 a0002c0002t0001g0181 a0002c0002t0001g0187 |
3 | HG01099.hp1 HG01361.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1012-41G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 10/39 | chr10 | 102359226 | |||||||
chr10:102359615 | C | T | 4 | a0001c0001t0003g0283 a0001c0001t0003g0284 a0001c0001t0003g0285 others(1): Show |
4 | NA18950.hp2 NA18979.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180+180C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 11/39 | chr10 | 102359615 | |||||||
chr10:102359757 | A | G | 1 | a0001c0014t0001g0166 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1180+322A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 11/39 | chr10 | 102359757 | |||||||
chr10:102359778 | C | CT | 71 | a0001c0001t0001g0136 a0001c0001t0001g0212 a0001c0001t0001g0213 others(68): Show |
71 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.1180+358dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 11/39 | INFO_REALIGN_3_PRIME | chr10 | 102359778 | ||||||
chr10:102359947 | G | A | 2 | a0001c0001t0002g0051 a0001c0001t0002g0062 |
2 | HG00280.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1181-237G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 11/39 | chr10 | 102359947 | |||||||
chr10:102360058 | G | A | 1 | a0001c0001t0001g0179 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1181-126G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 11/39 | chr10 | 102360058 | |||||||
chr10:102360461 | G | A | 1 | a0001c0001t0001g0125 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1392+66G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 12/39 | chr10 | 102360461 | |||||||
chr10:102360631 | C | G | 3 | a0001c0001t0002g0032 a0001c0001t0002g0033 a0001c0001t0002g0038 |
3 | HG02523.hp2 NA19004.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.1392+236C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 12/39 | chr10 | 102360631 | |||||||
chr10:102360728 | A | G | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1393-294A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 12/39 | chr10 | 102360728 | |||||||
chr10:102360765 | C | G | 58 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(55): Show |
58 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.1393-257C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 12/39 | chr10 | 102360765 | |||||||
chr10:102360929 | T | C | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1393-93T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 12/39 | chr10 | 102360929 | |||||||
chr10:102360974 | C | CA | 15 | a0001c0001t0001g0154 a0001c0001t0001g0213 a0001c0001t0001g0254 others(12): Show |
15 | HG00544.hp1 HG00738.hp1 HG01258.hp1 others(12): Show |
intron_variant | MODIFIER | c.1393-30dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 12/39 | INFO_REALIGN_3_PRIME | chr10 | 102360974 | ||||||
chr10:102361282 | T | C | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1491+162T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 13/39 | chr10 | 102361282 | |||||||
chr10:102361345 | T | C | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1491+225T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 13/39 | chr10 | 102361345 | |||||||
chr10:102361364 | G | A | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1491+244G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 13/39 | chr10 | 102361364 | |||||||
chr10:102361374 | C | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0151 |
2 | HG00738.hp2 HG01192.hp2 |
intron_variant | MODIFIER | c.1491+254C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 13/39 | chr10 | 102361374 | |||||||
chr10:102362050 | C | CT | 34 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0110 others(31): Show |
34 | HG00544.hp2 HG00609.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.1686+162dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/39 | INFO_REALIGN_3_PRIME | chr10 | 102362050 | ||||||
chr10:102362050 | CT | C | 96 | a0001c0001t0001g0126 a0001c0001t0001g0207 a0001c0001t0001g0208 others(93): Show |
96 | HG00099.hp2 HG00558.hp1 HG00621.hp2 others(93): Show |
intron_variant | MODIFIER | c.1686+162delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/39 | INFO_REALIGN_3_PRIME | chr10 | 102362050 | ||||||
chr10:102362050 | CTT | C | 7 | a0001c0001t0002g0028 a0001c0004t0002g0103 a0001c0004t0004g0001 others(4): Show |
8 | HG02280.hp1 HG02486.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.1686+161_1686+162d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/39 | INFO_REALIGN_3_PRIME | chr10 | 102362050 | ||||||
chr10:102362055 | T | C | 2 | a0001c0001t0002g0051 a0001c0001t0002g0062 |
2 | HG00280.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.1686+143T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/39 | chr10 | 102362055 | |||||||
chr10:102362057 | T | C | 1 | a0001c0001t0002g0013 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1686+145T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/39 | chr10 | 102362057 | |||||||
chr10:102362098 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1686+186C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/39 | chr10 | 102362098 | |||||||
chr10:102362158 | A | G | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.1686+246A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/39 | chr10 | 102362158 | |||||||
chr10:102362182 | G | A | 1 | a0001c0007t0001g0328 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1686+270G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/39 | chr10 | 102362182 | |||||||
chr10:102362217 | C | T | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1687-258C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/39 | chr10 | 102362217 | |||||||
chr10:102362355 | C | T | 1 | a0008c0018t0001g0204 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1687-120C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 14/39 | chr10 | 102362355 | |||||||
chr10:102362682 | C | A | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1876+18C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 15/39 | chr10 | 102362682 | |||||||
chr10:102362918 | T | G | 1 | a0001c0001t0003g0264 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1876+254T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 15/39 | chr10 | 102362918 | |||||||
chr10:102363085 | A | G | 59 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(56): Show |
59 | HG00099.hp2 HG00280.hp2 HG00673.hp1 others(56): Show |
intron_variant | MODIFIER | c.1877-171A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 15/39 | chr10 | 102363085 | |||||||
chr10:102363144 | C | T | 4 | a0001c0001t0002g0018 a0001c0001t0002g0058 a0001c0001t0002g0065 others(1): Show |
4 | HG01069.hp2 HG01071.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.1877-112C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 15/39 | chr10 | 102363144 | |||||||
chr10:102364012 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2106+214C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364012 | |||||||
chr10:102364123 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2106+325A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364123 | |||||||
chr10:102364166 | TTAGTAAG others(7): Show |
T | 1 | a0006c0015t0002g0061 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.2106+385_2106+398d others(16): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | INFO_REALIGN_3_PRIME | chr10 | 102364166 | ||||||
chr10:102364217 | C | CT | 137 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(134): Show |
138 | HG00099.hp1 HG00544.hp1 HG00609.hp2 others(135): Show |
intron_variant | MODIFIER | c.2106+444dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | INFO_REALIGN_3_PRIME | chr10 | 102364217 | ||||||
chr10:102364217 | C | CTT | 14 | a0001c0001t0001g0105 a0001c0001t0001g0190 a0001c0001t0001g0230 others(11): Show |
14 | HG00609.hp1 HG00735.hp2 HG02922.hp1 others(11): Show |
intron_variant | MODIFIER | c.2106+443_2106+444d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | INFO_REALIGN_3_PRIME | chr10 | 102364217 | ||||||
chr10:102364217 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0003g0258 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2106+434_2106+444d others(13): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | INFO_REALIGN_3_PRIME | chr10 | 102364217 | ||||||
chr10:102364228 | T | C | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2106+430T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364228 | |||||||
chr10:102364298 | C | G | 49 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0153 others(46): Show |
49 | HG00280.hp1 HG00544.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.2106+500C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364298 | |||||||
chr10:102364317 | CG | C | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2106+522delG | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | INFO_REALIGN_3_PRIME | chr10 | 102364317 | ||||||
chr10:102364320 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2106+522G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364320 | |||||||
chr10:102364438 | G | A | 3 | a0001c0001t0001g0243 a0001c0001t0001g0247 a0001c0001t0002g0013 |
3 | HG01256.hp1 HG01258.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.2106+640G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364438 | |||||||
chr10:102364517 | T | C | 320 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(317): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.2106+719T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364517 | |||||||
chr10:102364614 | C | T | 13 | a0001c0001t0001g0207 a0001c0003t0001g0108 a0001c0003t0001g0206 others(10): Show |
13 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.2107-783C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364614 | |||||||
chr10:102364848 | C | T | 58 | a0001c0001t0001g0008 a0001c0001t0001g0105 a0001c0001t0001g0106 others(55): Show |
58 | HG00280.hp1 HG00544.hp1 HG00609.hp2 others(55): Show |
intron_variant | MODIFIER | c.2107-549C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364848 | |||||||
chr10:102364961 | G | C | 5 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0296 others(2): Show |
5 | HG02559.hp1 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.2107-436G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364961 | |||||||
chr10:102364980 | C | T | 12 | a0001c0003t0001g0108 a0001c0003t0001g0206 a0001c0003t0001g0209 others(9): Show |
12 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(9): Show |
intron_variant | MODIFIER | c.2107-417C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102364980 | |||||||
chr10:102365264 | C | G | 1 | a0001c0001t0002g0091 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2107-133C>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 17/39 | chr10 | 102365264 | |||||||
chr10:102365648 | T | C | 1 | a0002c0002t0001g0205 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2309+49T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102365648 | |||||||
chr10:102365874 | GTGATAGA others(32): Show |
G | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2309+276_2309+314d others(41): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102365874 | |||||||
chr10:102365918 | G | C | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2309+319G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102365918 | |||||||
chr10:102365919 | T | C | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2309+320T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102365919 | |||||||
chr10:102365920 | G | A | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2309+321G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102365920 | |||||||
chr10:102365923 | A | C | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2309+324A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102365923 | |||||||
chr10:102365924 | G | C | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2309+325G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102365924 | |||||||
chr10:102365925 | A | G | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2309+326A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102365925 | |||||||
chr10:102365926 | GCT | G | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2309+328_2309+329d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102365926 | |||||||
chr10:102365951 | C | CA | 6 | a0001c0001t0001g0207 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2309+364dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | INFO_REALIGN_3_PRIME | chr10 | 102365951 | ||||||
chr10:102366017 | G | A | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2310-366G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102366017 | |||||||
chr10:102366097 | G | A | 1 | a0001c0001t0001g0236 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2310-286G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 18/39 | chr10 | 102366097 | |||||||
chr10:102366584 | C | CT | 22 | a0001c0001t0001g0006 a0001c0001t0001g0114 a0001c0001t0001g0118 others(19): Show |
23 | HG00099.hp1 HG00642.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.2433+98dupT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 19/39 | INFO_REALIGN_3_PRIME | chr10 | 102366584 | ||||||
chr10:102366584 | CT | C | 93 | a0001c0001t0001g0131 a0001c0001t0001g0159 a0001c0001t0001g0212 others(90): Show |
93 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.2433+98delT | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 19/39 | INFO_REALIGN_3_PRIME | chr10 | 102366584 | ||||||
chr10:102366680 | G | A | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.2433+174G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 19/39 | chr10 | 102366680 | |||||||
chr10:102366829 | G | A | 1 | a0001c0003t0001g0224 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2434-256G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 19/39 | chr10 | 102366829 | |||||||
chr10:102367257 | G | C | 1 | a0001c0001t0001g0141 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2559+47G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 20/39 | chr10 | 102367257 | |||||||
chr10:102367414 | G | A | 199 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(196): Show |
200 | HG00099.hp1 HG00280.hp1 HG00544.hp1 others(197): Show |
intron_variant | MODIFIER | c.2560-64G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 20/39 | chr10 | 102367414 | |||||||
chr10:102367979 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2643-239A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 21/39 | chr10 | 102367979 | |||||||
chr10:102368183 | G | A | 1 | a0001c0001t0001g0293 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2643-35G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 21/39 | chr10 | 102368183 | |||||||
chr10:102368633 | T | C | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.2880-106T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 22/39 | chr10 | 102368633 | |||||||
chr10:102369197 | T | A | 320 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(317): Show |
322 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.2974-14T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 23/39 | chr10 | 102369197 | |||||||
chr10:102369398 | G | A | 1 | a0002c0002t0001g0176 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.3150+11G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 24/39 | chr10 | 102369398 | |||||||
chr10:102370112 | T | G | 1 | a0001c0001t0003g0259 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3340-62T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 26/39 | chr10 | 102370112 | |||||||
chr10:102370551 | G | A | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3506+73G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 28/39 | chr10 | 102370551 | |||||||
chr10:102370942 | C | A | 1 | a0001c0001t0003g0282 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.3660+82C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102370942 | |||||||
chr10:102370986 | C | T | 1 | a0001c0001t0003g0268 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.3660+126C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102370986 | |||||||
chr10:102371017 | C | T | 1 | a0001c0001t0002g0033 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.3660+157C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102371017 | |||||||
chr10:102371329 | G | T | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.3660+469G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102371329 | |||||||
chr10:102371387 | A | G | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.3660+527A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102371387 | |||||||
chr10:102371546 | G | C | 2 | a0001c0001t0006g0164 a0001c0001t0006g0165 |
2 | HG03927.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.3660+686G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102371546 | |||||||
chr10:102371727 | A | G | 325 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(322): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.3660+867A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102371727 | |||||||
chr10:102371952 | G | C | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3660+1092G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102371952 | |||||||
chr10:102371994 | G | C | 123 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0109 others(120): Show |
124 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(121): Show |
intron_variant | MODIFIER | c.3660+1134G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102371994 | |||||||
chr10:102372032 | G | T | 1 | a0001c0001t0003g0235 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3660+1172G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102372032 | |||||||
chr10:102372142 | C | T | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3660+1282C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102372142 | |||||||
chr10:102372496 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.3660+1636C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102372496 | |||||||
chr10:102372716 | T | C | 1 | a0001c0001t0003g0283 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3660+1856T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102372716 | |||||||
chr10:102372778 | A | G | 82 | a0001c0001t0001g0190 a0001c0001t0001g0230 a0001c0001t0001g0236 others(79): Show |
83 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.3660+1918A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102372778 | |||||||
chr10:102373044 | A | G | 1 | a0002c0002t0001g0172 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.3660+2184A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102373044 | |||||||
chr10:102373435 | G | A | 1 | a0001c0001t0003g0265 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3661-1924G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102373435 | |||||||
chr10:102373498 | C | T | 1 | a0002c0002t0001g0187 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3661-1861C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102373498 | |||||||
chr10:102374347 | C | CA | 88 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(85): Show |
88 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.3661-1001dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | INFO_REALIGN_3_PRIME | chr10 | 102374347 | ||||||
chr10:102374695 | A | C | 1 | a0001c0001t0001g0182 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.3661-664A>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102374695 | |||||||
chr10:102374827 | T | G | 6 | a0001c0004t0002g0103 a0001c0004t0004g0001 a0001c0004t0004g0005 others(3): Show |
7 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.3661-532T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | chr10 | 102374827 | |||||||
chr10:102375202 | G | GA | 6 | a0001c0001t0001g0134 a0001c0001t0002g0017 a0001c0001t0002g0034 others(3): Show |
6 | HG01358.hp2 HG01928.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.3661-143dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 29/39 | INFO_REALIGN_3_PRIME | chr10 | 102375202 | ||||||
chr10:102375693 | C | T | 22 | a0001c0001t0001g0208 a0001c0001t0001g0214 a0001c0001t0001g0215 others(19): Show |
22 | HG01070.hp2 HG01081.hp1 HG01516.hp2 others(19): Show |
intron_variant | MODIFIER | c.3886+109C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102375693 | |||||||
chr10:102375826 | C | T | 3 | a0002c0002t0001g0171 a0002c0002t0001g0181 a0002c0002t0001g0187 |
3 | HG01099.hp1 HG01361.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.3886+242C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102375826 | |||||||
chr10:102375896 | T | TACTCGGG others(3): Show |
1 | a0003c0005t0002g0060 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3886+313_3886+314i others(12): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | INFO_REALIGN_3_PRIME | chr10 | 102375896 | ||||||
chr10:102375898 | G | T | 1 | a0003c0005t0002g0060 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3886+314G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102375898 | |||||||
chr10:102375901 | T | A | 1 | a0003c0005t0002g0060 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3886+317T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102375901 | |||||||
chr10:102375912 | G | C | 1 | a0003c0005t0002g0060 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3886+328G>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102375912 | |||||||
chr10:102375927 | A | G | 1 | a0003c0005t0002g0060 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3886+343A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102375927 | |||||||
chr10:102375929 | T | G | 1 | a0003c0005t0002g0060 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3887-343T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102375929 | |||||||
chr10:102375937 | T | G | 1 | a0003c0005t0002g0060 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3887-335T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102375937 | |||||||
chr10:102375939 | A | T | 1 | a0003c0005t0002g0060 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3887-333A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102375939 | |||||||
chr10:102375945 | T | A | 1 | a0003c0005t0002g0060 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.3887-327T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102375945 | |||||||
chr10:102376029 | A | G | 1 | a0001c0001t0003g0278 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3887-243A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102376029 | |||||||
chr10:102376222 | C | T | 2 | a0001c0003t0001g0226 a0001c0003t0001g0227 |
2 | HG02451.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.3887-50C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102376222 | |||||||
chr10:102376245 | C | T | 10 | a0001c0001t0002g0021 a0001c0001t0002g0026 a0001c0001t0002g0052 others(7): Show |
10 | NA18951.hp1 NA18955.hp1 NA18959.hp1 others(7): Show |
intron_variant | MODIFIER | c.3887-27C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 30/39 | chr10 | 102376245 | |||||||
chr10:102376859 | G | T | 2 | a0001c0001t0002g0085 a0001c0001t0002g0096 |
2 | HG03942.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.4288+59G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 32/39 | chr10 | 102376859 | |||||||
chr10:102377200 | C | T | 6 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0028 others(3): Show |
6 | HG01109.hp1 HG02055.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.4494+60C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102377200 | |||||||
chr10:102377318 | AATTTATT others(25): Show |
A | 90 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(87): Show |
90 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.4494+201_4494+232d others(34): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | INFO_REALIGN_3_PRIME | chr10 | 102377318 | ||||||
chr10:102377340 | T | A | 1 | a0001c0001t0003g0318 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.4494+200T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102377340 | |||||||
chr10:102377371 | T | A | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4494+231T>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102377371 | |||||||
chr10:102377383 | TCTCTCTG others(9): Show |
T | 3 | a0001c0001t0002g0023 a0001c0001t0002g0025 a0001c0001t0002g0047 |
3 | NA18944.hp2 NA18979.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.4494+246_4494+261d others(18): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | INFO_REALIGN_3_PRIME | chr10 | 102377383 | ||||||
chr10:102377456 | C | T | 5 | a0001c0001t0002g0027 a0001c0001t0002g0039 a0001c0001t0002g0040 others(2): Show |
5 | HG01934.hp2 HG01943.hp2 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.4494+316C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102377456 | |||||||
chr10:102377457 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.4494+317G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102377457 | |||||||
chr10:102377994 | T | C | 325 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(322): Show |
327 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(324): Show |
intron_variant | MODIFIER | c.4494+854T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102377994 | |||||||
chr10:102378090 | C | T | 1 | a0003c0005t0002g0076 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.4494+950C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102378090 | |||||||
chr10:102378135 | G | A | 2 | a0001c0001t0001g0178 a0001c0001t0001g0186 |
2 | NA19062.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.4494+995G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102378135 | |||||||
chr10:102378174 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.4494+1034T>C | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102378174 | |||||||
chr10:102378217 | C | CA | 12 | a0001c0001t0002g0033 a0001c0001t0002g0091 a0001c0001t0002g0092 others(9): Show |
13 | HG02071.hp2 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.4495-1053dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | INFO_REALIGN_3_PRIME | chr10 | 102378217 | ||||||
chr10:102378410 | G | T | 1 | a0001c0001t0001g0207 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4495-874G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102378410 | |||||||
chr10:102378589 | G | T | 1 | a0007c0011t0001g0294 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.4495-695G>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102378589 | |||||||
chr10:102378639 | AATAAAAT | A | 10 | a0001c0001t0001g0208 a0001c0001t0001g0214 a0001c0001t0001g0215 others(7): Show |
10 | HG02145.hp1 HG02559.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.4495-643_4495-637d others(9): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | INFO_REALIGN_3_PRIME | chr10 | 102378639 | ||||||
chr10:102378899 | A | T | 1 | a0002c0002t0001g0172 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4495-385A>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102378899 | |||||||
chr10:102378975 | A | G | 1 | a0001c0001t0006g0165 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4495-309A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102378975 | |||||||
chr10:102379239 | C | T | 7 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0111 others(4): Show |
7 | HG01106.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.4495-45C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 33/39 | chr10 | 102379239 | |||||||
chr10:102380774 | G | A | 1 | a0001c0004t0002g0103 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.5173+88G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 38/39 | chr10 | 102380774 | |||||||
chr10:102380845 | G | A | 89 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0002g0003 others(86): Show |
89 | HG00099.hp2 HG00280.hp2 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.5173+159G>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 38/39 | chr10 | 102380845 | |||||||
chr10:102381540 | C | T | 1 | a0001c0001t0003g0315 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.5302+285C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | chr10 | 102381540 | |||||||
chr10:102381814 | C | A | 1 | a0001c0001t0001g0292 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.5303-242C>A | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | chr10 | 102381814 | |||||||
chr10:102381815 | C | T | 1 | a0001c0001t0002g0033 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.5303-241C>T | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | chr10 | 102381815 | |||||||
chr10:102381822 | C | CGA | 73 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0128 others(70): Show |
74 | HG00099.hp1 HG00609.hp1 HG00642.hp2 others(71): Show |
intron_variant | MODIFIER | c.5303-233_5303-232d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | INFO_REALIGN_3_PRIME | chr10 | 102381822 | ||||||
chr10:102381823 | G | GA | 88 | a0001c0001t0001g0116 a0001c0001t0001g0154 a0001c0001t0001g0161 others(85): Show |
88 | HG00099.hp2 HG00280.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.5303-207dupA | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | INFO_REALIGN_3_PRIME | chr10 | 102381823 | ||||||
chr10:102381823 | G | GAGA | 12 | a0001c0001t0003g0241 a0001c0001t0003g0250 a0001c0001t0003g0265 others(9): Show |
12 | HG01981.hp2 HG02738.hp1 HG04115.hp1 others(9): Show |
intron_variant | MODIFIER | c.5303-232_5303-231i others(5): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | INFO_REALIGN_3_PRIME | chr10 | 102381823 | ||||||
chr10:102381823 | GAA | G | 5 | a0001c0004t0004g0001 a0001c0004t0004g0005 a0001c0004t0004g0014 others(2): Show |
6 | HG02280.hp1 HG02486.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.5303-208_5303-207d others(4): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | INFO_REALIGN_3_PRIME | chr10 | 102381823 | ||||||
chr10:102381823 | GAAAAAAA others(3): Show |
G | 1 | a0001c0001t0003g0268 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.5303-216_5303-207d others(12): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | INFO_REALIGN_3_PRIME | chr10 | 102381823 | ||||||
chr10:102381824 | A | AG | 3 | a0001c0001t0001g0008 a0001c0001t0003g0201 a0001c0001t0003g0307 |
3 | HG04204.hp1 NA19009.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.5303-232_5303-231i others(3): Show |
GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | chr10 | 102381824 | |||||||
chr10:102381835 | A | G | 1 | a0001c0001t0003g0268 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.5303-221A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | chr10 | 102381835 | |||||||
chr10:102381976 | T | G | 1 | a0001c0003t0001g0224 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.5303-80T>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | chr10 | 102381976 | |||||||
chr10:102381994 | A | G | 1 | a0001c0001t0001g0219 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.5303-62A>G | GBF1 | ENSG00000107862.7 | transcript | ENST00000369983.5 | protein_coding | 39/39 | chr10 | 102381994 |