Item | Value |
---|---|
geneid | 135152 |
ensemblid | ENSG00000112309.11 |
hgncid | 922 |
symbol | B3GAT2 |
name | beta-1,3-glucuronyltransferase 2 |
refseq_nuc | NM_080742.3 |
refseq_prot | NP_542780.1 |
ensembl_nuc | ENST00000230053.11 |
ensembl_prot | ENSP00000230053.6 |
mane_status | MANE Select |
chr | chr6 |
start | 70856679 |
end | 70957060 |
strand | - |
ver | v1.2 |
region | chr6:70856679-70957060 |
region5000 | chr6:70851679-70962060 |
regionname0 | B3GAT2_chr6_70856679_70957060 |
regionname5000 | B3GAT2_chr6_70851679_70962060 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 323 | 315 | 86 | 54 | 128 | 8 | 37 | 92 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | MKSAL others(318): Show |
chr6 | 70851679 | 70962060 |
a0002 | 0/0 | 323 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | MKSAL others(318): Show |
chr6 | 70851679 | 70962060 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 969 | 186 | 55 | 30 | 79 | 4 | 18 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | ATGAA others(964): Show |
chr6 | 70851679 | 70962060 | ||
a0001c0002 | 1/1 | 969 | 128 | 30 | 24 | 49 | 4 | 19 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | ATGAA others(964): Show |
chr6 | 70851679 | 70962060 | ||
a0001c0003 | 0/0 | 969 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | ATGAA others(964): Show |
chr6 | 70851679 | 70962060 | ||
a0002c0004 | 0/0 | 969 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | ATGAA others(964): Show |
chr6 | 70851679 | 70962060 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6586 | 25 | 1 | 4 | 12 | 1 | 7 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0002 | 0/0 | 6587 | 22 | 0 | 0 | 22 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0003 | 0/0 | 6586 | 21 | 7 | 2 | 7 | 0 | 5 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0004 | 0/0 | 6587 | 14 | 11 | 1 | 1 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0009 | 0/0 | 6587 | 7 | 1 | 3 | 3 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0010 | 0/0 | 6586 | 7 | 1 | 2 | 3 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0012 | 0/0 | 6587 | 6 | 2 | 0 | 4 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0013 | 0/0 | 6586 | 6 | 0 | 2 | 4 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0017 | 0/0 | 6586 | 4 | 0 | 3 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0018 | 0/0 | 6586 | 4 | 1 | 3 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0019 | 0/0 | 6586 | 4 | 0 | 1 | 3 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0020 | 0/0 | 6586 | 4 | 0 | 2 | 0 | 1 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0023 | 0/0 | 6584 | 3 | 3 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6579): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0024 | 0/0 | 6588 | 3 | 3 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6583): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0025 | 0/0 | 6587 | 3 | 2 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0032 | 0/0 | 6588 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6583): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0033 | 0/0 | 6587 | 2 | 2 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0034 | 0/0 | 6585 | 2 | 1 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6580): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0035 | 0/0 | 6586 | 2 | 0 | 1 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0036 | 0/0 | 6584 | 2 | 2 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6579): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0037 | 0/0 | 6587 | 2 | 0 | 0 | 0 | 0 | 2 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0044 | 0/0 | 6586 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0045 | 0/0 | 6597 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6592): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0046 | 0/0 | 6586 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0047 | 0/0 | 6586 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0048 | 0/0 | 6586 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0049 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6579): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0050 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0051 | 0/0 | 6587 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0052 | 0/0 | 6591 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6586): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0053 | 0/0 | 6586 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0054 | 0/0 | 6586 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0055 | 0/0 | 6585 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6580): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0056 | 0/0 | 6587 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0057 | 0/0 | 6588 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6583): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0058 | 0/0 | 6585 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6580): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0059 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6583): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0060 | 0/0 | 6588 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6583): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0061 | 0/0 | 6575 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6570): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0064 | 0/0 | 6585 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6580): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0065 | 0/0 | 6585 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6580): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0066 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6583): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0067 | 0/0 | 6587 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0068 | 0/0 | 6583 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6578): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0069 | 0/0 | 6587 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0070 | 0/0 | 6583 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6578): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0071 | 0/0 | 6591 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6586): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0072 | 0/0 | 6590 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6585): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0073 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6583): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0074 | 0/0 | 6588 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6583): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0075 | 0/0 | 6568 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6563): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0076 | 0/0 | 6586 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0102 | 0/0 | 6587 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0103 | 0/0 | 6586 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0104 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0105 | 0/0 | 6586 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0107 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0108 | 0/0 | 6588 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6583): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0109 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0110 | 0/0 | 6586 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0001t0111 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0005 | 0/0 | 6586 | 13 | 1 | 3 | 8 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0006 | 0/0 | 6587 | 10 | 6 | 0 | 3 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0007 | 0/0 | 6586 | 9 | 1 | 0 | 6 | 0 | 2 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0008 | 0/0 | 6586 | 8 | 0 | 6 | 0 | 0 | 2 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0011 | 0/0 | 6587 | 7 | 6 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0014 | 0/0 | 6586 | 6 | 0 | 5 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0015 | 0/0 | 6586 | 6 | 0 | 3 | 0 | 1 | 2 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0016 | 0/0 | 6586 | 5 | 0 | 0 | 3 | 0 | 2 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0021 | 0/0 | 6586 | 4 | 0 | 0 | 4 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0022 | 0/0 | 6587 | 4 | 0 | 1 | 3 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0026 | 0/0 | 6588 | 3 | 0 | 0 | 3 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6583): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0027 | 1/0 | 6587 | 3 | 0 | 0 | 0 | 2 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0028 | 0/0 | 6587 | 3 | 2 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0029 | 0/0 | 6586 | 3 | 0 | 1 | 1 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0030 | 0/0 | 6586 | 3 | 0 | 0 | 3 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0031 | 0/1 | 6587 | 3 | 1 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0038 | 0/0 | 6586 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0039 | 0/0 | 6587 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0040 | 0/0 | 6588 | 2 | 0 | 1 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6583): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0041 | 0/0 | 6587 | 2 | 2 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0042 | 0/0 | 6587 | 2 | 2 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0043 | 0/0 | 6586 | 2 | 2 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0077 | 0/0 | 6586 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0078 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0079 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0080 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6579): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0081 | 0/0 | 6587 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0082 | 0/0 | 6586 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0083 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0084 | 0/0 | 6577 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6572): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0085 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6583): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0086 | 0/0 | 6585 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6580): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0087 | 0/0 | 6568 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6563): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0088 | 0/0 | 6586 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0089 | 0/0 | 6585 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6580): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0090 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0091 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6579): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0092 | 0/0 | 6588 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6583): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0093 | 0/0 | 6587 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0094 | 0/0 | 6585 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6580): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0095 | 0/0 | 6585 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6580): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0096 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6583): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0097 | 0/0 | 6586 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0098 | 0/0 | 6587 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6582): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0099 | 0/0 | 6585 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6580): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0100 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6579): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0101 | 0/0 | 6584 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6579): Show |
chr6 | 70851679 | 70962060 |
a0001c0002t0106 | 0/0 | 6586 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0001c0003t0062 | 0/0 | 6586 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6581): Show |
chr6 | 70851679 | 70962060 |
a0002c0004t0063 | 0/0 | 6577 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | GCTGC others(6572): Show |
chr6 | 70851679 | 70962060 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0003g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0003g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0003g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0003g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0003g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0003g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0004g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0004g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0004g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0004g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0004g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0004g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0004g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0009g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0009g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0009g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0009g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0009g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0009g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0009g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0010g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0010g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0010g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0010g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0010g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0010g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0010g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0012g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0012g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0012g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0012g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0012g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0012g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0013g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0013g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0013g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0013g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0013g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0013g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0017g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0017g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0017g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0017g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0018g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0018g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0018g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0018g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0019g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0019g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0019g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0019g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0020g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0020g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0020g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0020g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0023g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0023g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0023g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0024g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0024g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0024g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0025g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0025g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0025g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0032g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0032g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0033g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0033g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0034g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0034g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0035g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0035g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0036g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0036g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0037g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0037g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0044g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0044g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0045g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0046g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0047g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0048g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0049g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0050g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0051g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0052g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0053g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0054g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0055g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0056g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0057g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0058g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0059g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0060g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0061g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0064g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0065g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0066g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0067g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0068g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0069g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0070g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0071g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0072g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0073g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0074g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0075g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0076g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0102g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0103g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0104g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0105g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0107g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0108g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0109g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0110g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0001t0111g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0005g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0005g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0005g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0005g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0005g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0005g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0005g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0005g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0006g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0006g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0006g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0006g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0007g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0007g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0007g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0007g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0007g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0007g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0007g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0007g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0007g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0008g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0008g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0008g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0008g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0008g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0008g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0008g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0011g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0011g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0011g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0011g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0011g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0011g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0011g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0014g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0014g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0014g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0014g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0014g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0014g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0015g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0015g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0015g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0015g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0015g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0015g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0016g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0016g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0016g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0016g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0016g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0021g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0021g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0021g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0021g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0022g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0022g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0022g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0022g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0026g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0026g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0026g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0027g0192 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0027g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0027g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0028g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0028g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0028g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0029g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0029g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0029g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0030g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0030g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0030g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0031g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0031g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0031g0293 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0038g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0038g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0039g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0039g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0040g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0040g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0041g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0041g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0042g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0042g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0043g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0043g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0077g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0078g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0079g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0080g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0081g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0082g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0083g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0084g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0085g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0086g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0087g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0088g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0089g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0090g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0091g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0092g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0093g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0094g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0095g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0096g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0097g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0098g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0099g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0100g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0101g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0002t0106g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0001c0003t0062g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
a0002c0004t0063g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0094 | g0274 | EUR | GBR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | GBR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00323 | hp1 | a0001 | c0002 | t0015 | g0280 | EUR | FIN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00323 | hp2 | a0001 | c0001 | t0004 | g0099 | EUR | FIN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00408 | hp2 | a0001 | c0001 | t0010 | g0124 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00423 | hp2 | a0001 | c0002 | t0078 | g0206 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00544 | hp2 | a0001 | c0001 | t0009 | g0160 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00597 | hp1 | a0001 | c0001 | t0013 | g0050 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00597 | hp2 | a0001 | c0002 | t0016 | g0236 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00621 | hp1 | a0001 | c0002 | t0087 | g0235 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00621 | hp2 | a0001 | c0002 | t0007 | g0203 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00642 | hp1 | a0001 | c0002 | t0014 | g0288 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00642 | hp2 | a0001 | c0002 | t0040 | g0222 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00673 | hp2 | a0001 | c0001 | t0012 | g0031 | EAS | CHS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00735 | hp1 | a0001 | c0001 | t0044 | g0303 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00735 | hp2 | a0001 | c0002 | t0008 | g0220 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00738 | hp1 | a0001 | c0002 | t0008 | g0003 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00738 | hp2 | a0001 | c0002 | t0014 | g0291 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00741 | hp1 | a0001 | c0001 | t0004 | g0126 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG00741 | hp2 | a0001 | c0002 | t0014 | g0278 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01069 | hp1 | a0001 | c0001 | t0025 | g0110 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01069 | hp2 | a0001 | c0002 | t0095 | g0282 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01071 | hp1 | a0001 | c0002 | t0014 | g0283 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01071 | hp2 | a0001 | c0002 | t0005 | g0225 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01074 | hp1 | a0001 | c0001 | t0019 | g0018 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01074 | hp2 | a0001 | c0002 | t0099 | g0290 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01099 | hp1 | a0001 | c0002 | t0015 | g0277 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01099 | hp2 | a0001 | c0002 | t0082 | g0238 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01167 | hp1 | a0001 | c0001 | t0003 | g0103 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01167 | hp2 | a0001 | c0002 | t0014 | g0286 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01168 | hp1 | a0001 | c0001 | t0035 | g0167 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01168 | hp2 | a0001 | c0002 | t0008 | g0218 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0127 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01169 | hp2 | a0001 | c0001 | t0064 | g0166 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01192 | hp1 | a0001 | c0002 | t0084 | g0243 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01255 | hp1 | a0001 | c0001 | t0017 | g0019 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01255 | hp2 | a0001 | c0002 | t0008 | g0003 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01256 | hp1 | a0001 | c0001 | t0013 | g0097 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01256 | hp2 | a0001 | c0001 | t0018 | g0013 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01257 | hp1 | a0001 | c0001 | t0018 | g0015 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01257 | hp2 | a0001 | c0001 | t0044 | g0305 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01261 | hp1 | a0001 | c0001 | t0010 | g0085 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01261 | hp2 | a0001 | c0001 | t0103 | g0307 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01346 | hp1 | a0001 | c0002 | t0015 | g0285 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01346 | hp2 | a0001 | c0001 | t0018 | g0014 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01433 | hp1 | a0001 | c0001 | t0020 | g0054 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01433 | hp2 | a0001 | c0002 | t0029 | g0279 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01496 | hp1 | a0001 | c0002 | t0005 | g0199 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01496 | hp2 | a0001 | c0002 | t0008 | g0215 | AMR | CLM | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01517 | hp1 | a0001 | c0001 | t0035 | g0045 | EUR | IBS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01517 | hp2 | a0001 | c0002 | t0027 | g0219 | EUR | IBS | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01884 | hp1 | a0001 | c0002 | t0011 | g0271 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0137 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01891 | hp1 | a0001 | c0002 | t0005 | g0200 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01891 | hp2 | a0001 | c0001 | t0010 | g0052 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01934 | hp2 | a0001 | c0002 | t0022 | g0281 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01952 | hp2 | a0001 | c0001 | t0013 | g0086 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01975 | hp1 | a0001 | c0001 | t0010 | g0072 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01975 | hp2 | a0001 | c0001 | t0020 | g0098 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01978 | hp1 | a0001 | c0001 | t0009 | g0048 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01978 | hp2 | a0001 | c0002 | t0005 | g0181 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01981 | hp1 | a0001 | c0002 | t0008 | g0227 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01981 | hp2 | a0001 | c0001 | t0017 | g0020 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01993 | hp1 | a0001 | c0001 | t0065 | g0068 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02004 | hp1 | a0001 | c0001 | t0009 | g0084 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02004 | hp2 | a0001 | c0001 | t0017 | g0029 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02015 | hp1 | a0001 | c0001 | t0010 | g0095 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02027 | hp1 | a0001 | c0001 | t0012 | g0023 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02027 | hp2 | a0001 | c0002 | t0021 | g0237 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02040 | hp1 | a0001 | c0002 | t0026 | g0208 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02055 | hp1 | a0001 | c0001 | t0024 | g0130 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02055 | hp2 | a0001 | c0001 | t0009 | g0096 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02056 | hp1 | a0001 | c0001 | t0013 | g0034 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02071 | hp1 | a0001 | c0001 | t0111 | g0313 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02071 | hp2 | a0001 | c0002 | t0007 | g0211 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0145 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02129 | hp2 | a0001 | c0002 | t0021 | g0230 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02132 | hp1 | a0001 | c0002 | t0030 | g0301 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02132 | hp2 | a0001 | c0002 | t0079 | g0201 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02135 | hp1 | a0001 | c0002 | t0022 | g0265 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02135 | hp2 | a0001 | c0001 | t0004 | g0149 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02145 | hp1 | a0001 | c0002 | t0031 | g0276 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02145 | hp2 | a0001 | c0001 | t0024 | g0041 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02155 | hp1 | a0001 | c0002 | t0021 | g0248 | EAS | CDX | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02155 | hp2 | a0001 | c0001 | t0012 | g0028 | EAS | CDX | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02165 | hp1 | a0001 | c0002 | t0006 | g0234 | EAS | CDX | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02165 | hp2 | a0001 | c0001 | t0060 | g0120 | EAS | CDX | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02258 | hp1 | a0001 | c0001 | t0024 | g0125 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0057 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02280 | hp1 | a0001 | c0001 | t0051 | g0006 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0133 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02300 | hp1 | a0001 | c0001 | t0009 | g0093 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02300 | hp2 | a0001 | c0002 | t0015 | g0252 | AMR | PEL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02451 | hp1 | a0001 | c0001 | t0018 | g0007 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0128 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02523 | hp1 | a0001 | c0001 | t0010 | g0040 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02523 | hp2 | a0001 | c0001 | t0012 | g0026 | EAS | KHV | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02572 | hp1 | a0001 | c0002 | t0080 | g0194 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0132 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02602 | hp1 | a0001 | c0002 | t0106 | g0308 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02602 | hp2 | a0001 | c0002 | t0081 | g0239 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02622 | hp1 | a0001 | c0002 | t0006 | g0188 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02622 | hp2 | a0001 | c0001 | t0102 | g0302 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02630 | hp1 | a0001 | c0002 | t0006 | g0187 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02630 | hp2 | a0001 | c0001 | t0012 | g0011 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02647 | hp1 | a0001 | c0002 | t0041 | g0196 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02647 | hp2 | a0001 | c0002 | t0100 | g0256 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02683 | hp1 | a0001 | c0001 | t0010 | g0158 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02698 | hp2 | a0002 | c0004 | t0063 | g0175 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02717 | hp1 | a0001 | c0001 | t0069 | g0104 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02717 | hp2 | a0001 | c0002 | t0011 | g0255 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02723 | hp1 | a0001 | c0002 | t0041 | g0189 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02723 | hp2 | a0001 | c0001 | t0049 | g0012 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02735 | hp1 | a0001 | c0002 | t0008 | g0247 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02735 | hp2 | a0001 | c0002 | t0015 | g0287 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02738 | hp1 | a0001 | c0002 | t0088 | g0296 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02738 | hp2 | a0001 | c0002 | t0028 | g0251 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02809 | hp1 | a0001 | c0001 | t0004 | g0165 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02809 | hp2 | a0001 | c0002 | t0028 | g0195 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02818 | hp1 | a0001 | c0001 | t0053 | g0033 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02818 | hp2 | a0001 | c0001 | t0034 | g0107 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02886 | hp1 | a0001 | c0002 | t0028 | g0221 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02886 | hp2 | a0001 | c0001 | t0067 | g0114 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0139 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02895 | hp2 | a0001 | c0002 | t0101 | g0257 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02896 | hp1 | a0001 | c0001 | t0048 | g0009 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02896 | hp2 | a0001 | c0001 | t0004 | g0164 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02965 | hp1 | a0001 | c0002 | t0011 | g0261 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0113 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02970 | hp1 | a0001 | c0002 | t0006 | g0190 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02970 | hp2 | a0001 | c0001 | t0056 | g0116 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02976 | hp1 | a0001 | c0002 | t0091 | g0259 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02976 | hp2 | a0001 | c0001 | t0073 | g0108 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0134 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03041 | hp2 | a0001 | c0001 | t0036 | g0105 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03098 | hp1 | a0001 | c0002 | t0042 | g0294 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03098 | hp2 | a0001 | c0002 | t0011 | g0254 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03130 | hp1 | a0001 | c0002 | t0096 | g0260 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03130 | hp2 | a0001 | c0001 | t0004 | g0141 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03139 | hp1 | a0001 | c0002 | t0011 | g0258 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03139 | hp2 | a0001 | c0001 | t0023 | g0078 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03195 | hp1 | a0001 | c0001 | t0055 | g0131 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03195 | hp2 | a0001 | c0001 | t0054 | g0032 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03209 | hp1 | a0001 | c0001 | t0004 | g0162 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03209 | hp2 | a0001 | c0001 | t0070 | g0112 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03225 | hp1 | a0001 | c0002 | t0043 | g0272 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03225 | hp2 | a0001 | c0001 | t0033 | g0076 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03239 | hp1 | a0001 | c0001 | t0037 | g0062 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03239 | hp2 | a0001 | c0002 | t0008 | g0249 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03453 | hp1 | a0001 | c0002 | t0042 | g0253 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0140 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03486 | hp1 | a0001 | c0003 | t0062 | g0106 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03486 | hp2 | a0001 | c0002 | t0043 | g0273 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0169 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03491 | hp1 | a0001 | c0001 | t0020 | g0079 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03491 | hp2 | a0001 | c0002 | t0016 | g0228 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03492 | hp2 | a0001 | c0002 | t0016 | g0226 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03516 | hp1 | a0001 | c0001 | t0033 | g0115 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03516 | hp2 | a0001 | c0002 | t0006 | g0197 | AFR | ESN | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03540 | hp1 | a0001 | c0002 | t0007 | g0184 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03540 | hp2 | a0001 | c0001 | t0025 | g0138 | AFR | GWD | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0136 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03579 | hp2 | a0001 | c0002 | t0006 | g0186 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03654 | hp1 | a0001 | c0002 | t0005 | g0240 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03654 | hp2 | a0001 | c0002 | t0029 | g0275 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03669 | hp1 | a0001 | c0001 | t0074 | g0088 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03669 | hp2 | a0001 | c0001 | t0003 | g0100 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03688 | hp1 | a0001 | c0001 | t0003 | g0101 | SAS | STU | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0042 | SAS | STU | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03710 | hp2 | a0001 | c0001 | t0037 | g0089 | SAS | PJL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03831 | hp1 | a0001 | c0002 | t0014 | g0289 | SAS | BEB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03831 | hp2 | a0001 | c0002 | t0006 | g0245 | SAS | BEB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03834 | hp1 | a0001 | c0002 | t0007 | g0191 | SAS | BEB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03834 | hp2 | a0001 | c0002 | t0086 | g0183 | SAS | BEB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03927 | hp1 | a0001 | c0002 | t0097 | g0295 | SAS | BEB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG04184 | hp1 | a0001 | c0002 | t0015 | g0284 | SAS | BEB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0081 | SAS | BEB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG04199 | hp1 | a0001 | c0001 | t0047 | g0016 | SAS | STU | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG04199 | hp2 | a0001 | c0002 | t0007 | g0250 | SAS | STU | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0155 | SAS | STU | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG04204 | hp2 | a0001 | c0002 | t0098 | g0292 | SAS | STU | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18747 | hp1 | a0001 | c0002 | t0026 | g0180 | EAS | CHB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18747 | hp2 | a0001 | c0001 | t0046 | g0017 | EAS | CHB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18906 | hp1 | a0001 | c0002 | t0085 | g0198 | AFR | YRI | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18906 | hp2 | a0001 | c0001 | t0023 | g0087 | AFR | YRI | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0092 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18940 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18945 | hp1 | a0001 | c0001 | t0019 | g0025 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18945 | hp2 | a0001 | c0001 | t0071 | g0039 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18949 | hp1 | a0001 | c0002 | t0005 | g0231 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18951 | hp1 | a0001 | c0002 | t0092 | g0264 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18960 | hp1 | a0001 | c0001 | t0104 | g0304 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18960 | hp2 | a0001 | c0002 | t0005 | g0232 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0091 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18962 | hp2 | a0001 | c0002 | t0030 | g0263 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18963 | hp1 | a0001 | c0002 | t0005 | g0216 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18963 | hp2 | a0001 | c0001 | t0019 | g0024 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18964 | hp1 | a0001 | c0001 | t0050 | g0022 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18964 | hp2 | a0001 | c0001 | t0108 | g0312 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18965 | hp1 | a0001 | c0002 | t0093 | g0267 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18967 | hp1 | a0001 | c0001 | t0013 | g0117 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18969 | hp2 | a0001 | c0002 | t0006 | g0207 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18974 | hp1 | a0001 | c0002 | t0026 | g0242 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18974 | hp2 | a0001 | c0002 | t0031 | g0266 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18975 | hp2 | a0001 | c0002 | t0038 | g0177 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18980 | hp1 | a0001 | c0002 | t0040 | g0185 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18980 | hp2 | a0001 | c0001 | t0034 | g0148 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18981 | hp1 | a0001 | c0001 | t0032 | g0005 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18981 | hp2 | a0001 | c0002 | t0090 | g0300 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18984 | hp1 | a0001 | c0002 | t0030 | g0262 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18994 | hp2 | a0001 | c0002 | t0005 | g0210 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18997 | hp1 | a0001 | c0001 | t0052 | g0021 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18997 | hp2 | a0001 | c0001 | t0013 | g0129 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19000 | hp1 | a0001 | c0002 | t0083 | g0209 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0146 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19002 | hp1 | a0001 | c0001 | t0009 | g0118 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19002 | hp2 | a0001 | c0002 | t0007 | g0241 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19005 | hp2 | a0001 | c0002 | t0005 | g0202 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19006 | hp1 | a0001 | c0001 | t0003 | g0090 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19006 | hp2 | a0001 | c0001 | t0107 | g0311 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19007 | hp2 | a0001 | c0002 | t0006 | g0229 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19009 | hp1 | a0001 | c0001 | t0061 | g0094 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19009 | hp2 | a0001 | c0002 | t0022 | g0298 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19010 | hp1 | a0001 | c0002 | t0011 | g0269 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19011 | hp2 | a0001 | c0002 | t0007 | g0224 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19012 | hp1 | a0001 | c0002 | t0029 | g0299 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19012 | hp2 | a0001 | c0001 | t0072 | g0037 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19030 | hp1 | a0001 | c0001 | t0004 | g0075 | AFR | LWK | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19030 | hp2 | a0001 | c0001 | t0066 | g0143 | AFR | LWK | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19043 | hp1 | a0001 | c0001 | t0025 | g0111 | AFR | LWK | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19043 | hp2 | a0001 | c0002 | t0011 | g0270 | AFR | LWK | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19056 | hp1 | a0001 | c0002 | t0038 | g0179 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19056 | hp2 | a0001 | c0002 | t0039 | g0246 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19057 | hp1 | a0001 | c0001 | t0058 | g0083 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19057 | hp2 | a0001 | c0002 | t0005 | g0233 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19058 | hp1 | a0001 | c0002 | t0039 | g0204 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19058 | hp2 | a0001 | c0001 | t0076 | g0176 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19062 | hp2 | a0001 | c0002 | t0007 | g0223 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19064 | hp1 | a0001 | c0001 | t0057 | g0074 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19064 | hp2 | a0001 | c0002 | t0005 | g0217 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19065 | hp2 | a0001 | c0001 | t0032 | g0027 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19066 | hp1 | a0001 | c0002 | t0007 | g0213 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19066 | hp2 | a0001 | c0001 | t0110 | g0310 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19070 | hp2 | a0001 | c0002 | t0021 | g0182 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19078 | hp1 | a0001 | c0001 | t0017 | g0008 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19078 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19081 | hp1 | a0001 | c0001 | t0009 | g0156 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19082 | hp1 | a0001 | c0001 | t0019 | g0030 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19083 | hp1 | a0001 | c0002 | t0022 | g0268 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19083 | hp2 | a0001 | c0002 | t0005 | g0214 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19084 | hp1 | a0001 | c0002 | t0077 | g0178 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19085 | hp1 | a0001 | c0002 | t0016 | g0205 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA20752 | hp1 | a0001 | c0001 | t0020 | g0067 | EUR | TSI | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA20752 | hp2 | a0001 | c0002 | t0027 | g0212 | EUR | TSI | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02109 | hp1 | a0001 | c0001 | t0059 | g0163 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02109 | hp2 | a0001 | c0001 | t0036 | g0142 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0056 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0109 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02559 | hp1 | a0001 | c0001 | t0045 | g0004 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG02559 | hp2 | a0001 | c0002 | t0006 | g0193 | AFR | ACB | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0082 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG03471 | hp2 | a0001 | c0001 | t0012 | g0010 | AFR | MSL | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG06807 | hp1 | a0001 | c0001 | t0023 | g0077 | AFR | USA | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
HG06807 | hp2 | a0001 | c0001 | t0068 | g0168 | AFR | USA | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18955 | hp1 | a0001 | c0001 | t0109 | g0309 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA18955 | hp2 | a0001 | c0002 | t0016 | g0244 | EAS | JPT | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA20300 | hp1 | a0001 | c0001 | t0105 | g0306 | AFR | USA | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0053 | AFR | USA | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA21309 | hp1 | a0001 | c0001 | t0075 | g0135 | AFR | LWK | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
NA21309 | hp2 | a0001 | c0002 | t0089 | g0297 | AFR | LWK | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
homoSapiens | chm13v2 | a0001 | c0002 | t0031 | g0293 | REF | REF | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
homoSapiens | grch38p0 | a0001 | c0002 | t0027 | g0192 | REF | REF | B3GAT2_chr6_70851679_70962060 | B3GAT2 | chr6 | 70851679 | 70962060 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:70956279 | G | C | 1 | a0002 | 1 | HG02698.hp2 | missense_variant | MODERATE | c.151C>G | p.Arg51Gly | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 782/6587 | 151/972 | 51/323 | chr6 | 70956279 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:70861893 | A | G | 1 | a0001c0003 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.822T>C | p.Ser274Ser | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 3/4 | 1453/6587 | 822/972 | 274/323 | chr6 | 70861893 | |||
chr6:70956283 | G | A | 3 | a0001c0001 a0001c0003 a0002c0004 |
188 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(185): Show |
synonymous_variant | LOW | c.147C>T | p.Gly49Gly | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 778/6587 | 147/972 | 49/323 | chr6 | 70956283 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:70856766 | A | G | 1 | a0001c0002t0042 | 2 | HG03098.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4897T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 4897 | chr6 | 70856766 | ||||||
chr6:70856944 | C | G | 1 | a0001c0002t0100 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4719G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 4719 | chr6 | 70856944 | ||||||
chr6:70857845 | A | G | 2 | a0001c0001t0045 a0001c0002t0042 |
3 | HG02559.hp1 HG03098.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3818T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3818 | chr6 | 70857845 | ||||||
chr6:70857887 | GCT | G | 4 | a0001c0001t0036 a0001c0001t0068 a0001c0002t0100 others(1): Show |
5 | HG02109.hp2 HG02647.hp2 HG02895.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*3774_*3775delAG | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3774 | chr6 | 70857887 | ||||||
chr6:70857946 | T | C | 1 | a0001c0002t0093 | 1 | NA18965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3717A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3717 | chr6 | 70857946 | ||||||
chr6:70858014 | G | C | 1 | a0001c0002t0083 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3649C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3649 | chr6 | 70858014 | ||||||
chr6:70858287 | C | CT | 13 | a0001c0001t0024 a0001c0001t0032 a0001c0001t0057 others(10): Show |
19 | HG00642.hp2 HG02040.hp1 HG02055.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*3375dupA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3375 | chr6 | 70858287 | ||||||
chr6:70858287 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0045 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3366_*3375dupAAAA others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3375 | chr6 | 70858287 | ||||||
chr6:70858287 | CT | C | 42 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0010 others(39): Show |
162 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*3375delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3375 | chr6 | 70858287 | ||||||
chr6:70858287 | CTT | C | 11 | a0001c0001t0034 a0001c0001t0055 a0001c0001t0058 others(8): Show |
12 | HG00099.hp1 HG01069.hp2 HG01074.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*3374_*3375delAA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3374 | chr6 | 70858287 | ||||||
chr6:70858287 | CTTTT | C | 5 | a0001c0001t0023 a0001c0001t0049 a0001c0001t0070 others(2): Show |
7 | HG02572.hp1 HG02723.hp2 HG02976.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3372_*3375delAAAA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3372 | chr6 | 70858287 | ||||||
chr6:70858287 | CTTTTTTT others(3): Show |
C | 2 | a0001c0002t0084 a0002c0004t0063 |
2 | HG01192.hp1 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3366_*3375delAAAA others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3366 | chr6 | 70858287 | ||||||
chr6:70858287 | CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0061 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3364_*3375delAAAA others(8): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3364 | chr6 | 70858287 | ||||||
chr6:70858299 | T | G | 9 | a0001c0001t0010 a0001c0001t0019 a0001c0001t0103 others(6): Show |
22 | HG00408.hp2 HG01074.hp1 HG01099.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*3364A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3364 | chr6 | 70858299 | ||||||
chr6:70858338 | G | A | 4 | a0001c0001t0023 a0001c0001t0049 a0001c0002t0080 others(1): Show |
6 | HG02572.hp1 HG02723.hp2 HG02976.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3325C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3325 | chr6 | 70858338 | ||||||
chr6:70858427 | G | C | 98 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(95): Show |
273 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(270): Show |
3_prime_UTR_variant | MODIFIER | c.*3236C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 3236 | chr6 | 70858427 | ||||||
chr6:70858714 | A | G | 36 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0010 others(33): Show |
110 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(107): Show |
3_prime_UTR_variant | MODIFIER | c.*2949T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2949 | chr6 | 70858714 | ||||||
chr6:70858976 | A | G | 2 | a0001c0002t0084 a0002c0004t0063 |
2 | HG01192.hp1 HG02698.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2687T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2687 | chr6 | 70858976 | ||||||
chr6:70859049 | G | A | 2 | a0001c0001t0069 a0001c0001t0070 |
2 | HG02717.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2614C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2614 | chr6 | 70859049 | ||||||
chr6:70859138 | T | C | 23 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0010 others(20): Show |
77 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2525A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2525 | chr6 | 70859138 | ||||||
chr6:70859204 | G | A | 1 | a0001c0002t0080 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2459C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2459 | chr6 | 70859204 | ||||||
chr6:70859210 | A | T | 1 | a0001c0001t0050 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2453T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2453 | chr6 | 70859210 | ||||||
chr6:70859232 | A | G | 23 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0010 others(20): Show |
77 | HG00099.hp2 HG00408.hp2 HG00544.hp2 others(74): Show |
3_prime_UTR_variant | MODIFIER | c.*2431T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2431 | chr6 | 70859232 | ||||||
chr6:70859303 | G | C | 1 | a0001c0002t0080 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2360C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2360 | chr6 | 70859303 | ||||||
chr6:70859379 | C | T | 1 | a0001c0003t0062 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2284G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2284 | chr6 | 70859379 | ||||||
chr6:70859387 | T | C | 56 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0010 others(53): Show |
135 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(132): Show |
3_prime_UTR_variant | MODIFIER | c.*2276A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2276 | chr6 | 70859387 | ||||||
chr6:70859426 | C | T | 22 | a0001c0001t0002 a0001c0001t0012 a0001c0001t0032 others(19): Show |
58 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*2237G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2237 | chr6 | 70859426 | ||||||
chr6:70859483 | C | T | 2 | a0001c0001t0103 a0001c0002t0082 |
2 | HG01099.hp2 HG01261.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2180G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2180 | chr6 | 70859483 | ||||||
chr6:70859545 | T | TGTAA | 3 | a0001c0001t0052 a0001c0001t0071 a0001c0001t0072 |
3 | NA18945.hp2 NA18997.hp1 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2114_*2117dupTTAC | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 2117 | chr6 | 70859545 | ||||||
chr6:70860115 | A | G | 1 | a0001c0002t0081 | 1 | HG02602.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1548T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 1548 | chr6 | 70860115 | ||||||
chr6:70860310 | T | A | 1 | a0001c0001t0045 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1353A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 1353 | chr6 | 70860310 | ||||||
chr6:70860420 | A | AT | 5 | a0001c0001t0023 a0001c0001t0049 a0001c0001t0059 others(2): Show |
7 | HG02109.hp1 HG02572.hp1 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1242dupA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 1242 | chr6 | 70860420 | ||||||
chr6:70860773 | T | C | 1 | a0001c0002t0077 | 1 | NA19084.hp1 | 3_prime_UTR_variant | MODIFIER | c.*890A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 890 | chr6 | 70860773 | ||||||
chr6:70860938 | A | G | 16 | a0001c0001t0001 a0001c0001t0009 a0001c0001t0044 others(13): Show |
58 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*725T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 725 | chr6 | 70860938 | ||||||
chr6:70860956 | T | C | 1 | a0001c0001t0073 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*707A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 707 | chr6 | 70860956 | ||||||
chr6:70861042 | C | T | 1 | a0001c0001t0056 | 1 | HG02970.hp2 | 3_prime_UTR_variant | MODIFIER | c.*621G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 621 | chr6 | 70861042 | ||||||
chr6:70861177 | T | A | 2 | a0001c0001t0037 a0001c0001t0074 |
3 | HG03239.hp1 HG03669.hp1 HG03710.hp2 |
3_prime_UTR_variant | MODIFIER | c.*486A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 486 | chr6 | 70861177 | ||||||
chr6:70861178 | T | C | 2 | a0001c0001t0111 a0001c0002t0078 |
2 | HG00423.hp2 HG02071.hp1 |
3_prime_UTR_variant | MODIFIER | c.*485A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 485 | chr6 | 70861178 | ||||||
chr6:70861262 | C | T | 1 | a0001c0001t0055 | 1 | HG03195.hp1 | 3_prime_UTR_variant | MODIFIER | c.*401G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 401 | chr6 | 70861262 | ||||||
chr6:70861294 | AAACCTGT others(11): Show |
A | 2 | a0001c0001t0075 a0001c0002t0087 |
2 | HG00621.hp1 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*351_*368delGGTAGA others(12): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 351 | chr6 | 70861294 | ||||||
chr6:70861511 | C | G | 1 | a0001c0002t0078 | 1 | HG00423.hp2 | 3_prime_UTR_variant | MODIFIER | c.*152G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 152 | chr6 | 70861511 | ||||||
chr6:70861593 | C | G | 2 | a0001c0002t0088 a0001c0002t0089 |
2 | HG02738.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*70G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 70 | chr6 | 70861593 | ||||||
chr6:70861617 | A | T | 1 | a0001c0001t0033 | 2 | HG03225.hp2 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*46T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 46 | chr6 | 70861617 | ||||||
chr6:70861626 | C | T | 1 | a0001c0001t0046 | 1 | NA18747.hp2 | 3_prime_UTR_variant | MODIFIER | c.*37G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 37 | chr6 | 70861626 | ||||||
chr6:70861646 | C | T | 1 | a0001c0001t0053 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*17G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 4/4 | 17 | chr6 | 70861646 | ||||||
chr6:70956443 | T | C | 87 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(84): Show |
238 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(235): Show |
5_prime_UTR_variant | MODIFIER | c.-14A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 14 | chr6 | 70956443 | ||||||
chr6:70956511 | G | A | 2 | a0001c0001t0053 a0001c0001t0054 |
2 | HG02818.hp1 HG03195.hp2 |
5_prime_UTR_variant | MODIFIER | c.-82C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 82 | chr6 | 70956511 | ||||||
chr6:70956524 | G | A | 63 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(60): Show |
188 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(185): Show |
5_prime_UTR_variant | MODIFIER | c.-95C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 95 | chr6 | 70956524 | ||||||
chr6:70956676 | A | C | 2 | a0001c0002t0038 a0001c0002t0077 |
3 | NA18975.hp2 NA19056.hp1 NA19084.hp1 |
5_prime_UTR_variant | MODIFIER | c.-247T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 247 | chr6 | 70956676 | ||||||
chr6:70956697 | G | A | 1 | a0001c0001t0076 | 1 | NA19058.hp2 | 5_prime_UTR_variant | MODIFIER | c.-268C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 268 | chr6 | 70956697 | ||||||
chr6:70956842 | C | G | 63 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(60): Show |
188 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(185): Show |
5_prime_UTR_variant | MODIFIER | c.-413G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 413 | chr6 | 70956842 | ||||||
chr6:70956906 | C | T | 14 | a0001c0001t0012 a0001c0001t0017 a0001c0001t0018 others(11): Show |
29 | HG00673.hp2 HG01074.hp1 HG01255.hp1 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-477G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 477 | chr6 | 70956906 | ||||||
chr6:70956937 | C | A | 1 | a0001c0001t0102 | 1 | HG02622.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-508G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | chr6 | 70956937 | |||||||
chr6:70956942 | T | G | 4 | a0001c0001t0044 a0001c0001t0103 a0001c0001t0104 others(1): Show |
5 | HG00735.hp1 HG01257.hp2 HG01261.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-513A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 513 | chr6 | 70956942 | ||||||
chr6:70956954 | G | T | 1 | a0001c0001t0045 | 1 | HG02559.hp1 | 5_prime_UTR_variant | MODIFIER | c.-525C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 525 | chr6 | 70956954 | ||||||
chr6:70956987 | T | G | 1 | a0001c0002t0106 | 1 | HG02602.hp1 | 5_prime_UTR_variant | MODIFIER | c.-558A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | 558 | chr6 | 70956987 | ||||||
chr6:70957039 | G | C | 5 | a0001c0001t0107 a0001c0001t0108 a0001c0001t0109 others(2): Show |
5 | HG02071.hp1 NA18955.hp1 NA18964.hp2 others(2): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-610C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/4 | chr6 | 70957039 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:70861778 | C | T | 1 | a0001c0001t0109g0309 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.886-29G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 3/3 | chr6 | 70861778 | |||||||
chr6:70862002 | A | G | 2 | a0001c0001t0002g0059 a0001c0001t0012g0028 |
2 | HG02015.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.737-24T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70862002 | |||||||
chr6:70862061 | A | G | 1 | a0001c0001t0055g0131 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.737-83T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70862061 | |||||||
chr6:70862404 | T | A | 7 | a0001c0001t0023g0077 a0001c0001t0023g0078 a0001c0001t0066g0143 others(4): Show |
7 | HG02572.hp1 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.737-426A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70862404 | |||||||
chr6:70862789 | A | G | 1 | a0001c0002t0042g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.737-811T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70862789 | |||||||
chr6:70862863 | G | A | 1 | a0001c0002t0006g0197 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.737-885C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70862863 | |||||||
chr6:70862903 | T | C | 1 | a0001c0001t0003g0147 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.737-925A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70862903 | |||||||
chr6:70862965 | G | A | 1 | a0001c0002t0029g0275 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.737-987C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70862965 | |||||||
chr6:70863068 | C | T | 2 | a0001c0002t0084g0243 a0002c0004t0063g0175 |
2 | HG01192.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.737-1090G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70863068 | |||||||
chr6:70863107 | G | C | 1 | a0001c0001t0066g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.737-1129C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70863107 | |||||||
chr6:70863406 | G | A | 112 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(109): Show |
114 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(111): Show |
intron_variant | MODIFIER | c.737-1428C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70863406 | |||||||
chr6:70863672 | T | C | 5 | a0001c0001t0024g0041 a0001c0001t0024g0125 a0001c0001t0024g0130 others(2): Show |
5 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.737-1694A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70863672 | |||||||
chr6:70863853 | G | A | 3 | a0001c0001t0045g0004 a0001c0002t0042g0253 a0001c0002t0042g0294 |
3 | HG02559.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.737-1875C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70863853 | |||||||
chr6:70864053 | G | C | 1 | a0001c0001t0001g0170 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.737-2075C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70864053 | |||||||
chr6:70864061 | C | CT | 22 | a0001c0001t0020g0054 a0001c0001t0020g0067 a0001c0001t0020g0098 others(19): Show |
23 | HG00323.hp1 HG00735.hp2 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.737-2084dupA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70864061 | |||||||
chr6:70864061 | CT | C | 35 | a0001c0001t0002g0038 a0001c0001t0002g0059 a0001c0001t0002g0122 others(32): Show |
35 | HG00741.hp1 HG01169.hp1 HG01255.hp1 others(32): Show |
intron_variant | MODIFIER | c.737-2084delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70864061 | |||||||
chr6:70864061 | CTT | C | 61 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(58): Show |
62 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.737-2085_737-2084d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70864061 | |||||||
chr6:70864061 | CTTT | C | 20 | a0001c0001t0001g0144 a0001c0001t0001g0157 a0001c0001t0010g0095 others(17): Show |
20 | HG00408.hp2 HG01074.hp1 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.737-2086_737-2084d others(5): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70864061 | |||||||
chr6:70864666 | A | G | 62 | a0001c0001t0003g0036 a0001c0001t0003g0081 a0001c0001t0003g0082 others(59): Show |
62 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(59): Show |
intron_variant | MODIFIER | c.737-2688T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70864666 | |||||||
chr6:70864895 | C | T | 1 | a0001c0001t0055g0131 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.737-2917G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70864895 | |||||||
chr6:70864938 | A | G | 1 | a0001c0002t0014g0286 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.737-2960T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70864938 | |||||||
chr6:70865092 | A | G | 127 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(124): Show |
129 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.737-3114T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865092 | |||||||
chr6:70865252 | G | A | 3 | a0001c0001t0045g0004 a0001c0002t0042g0253 a0001c0002t0042g0294 |
3 | HG02559.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.737-3274C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865252 | |||||||
chr6:70865282 | C | G | 1 | a0001c0001t0004g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.737-3304G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865282 | |||||||
chr6:70865406 | C | T | 1 | a0001c0002t0043g0273 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.737-3428G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865406 | |||||||
chr6:70865483 | G | C | 1 | a0001c0001t0009g0096 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.737-3505C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865483 | |||||||
chr6:70865498 | G | A | 77 | a0001c0001t0002g0001 a0001c0001t0002g0035 a0001c0001t0002g0038 others(74): Show |
78 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.737-3520C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865498 | |||||||
chr6:70865536 | A | G | 1 | a0001c0002t0006g0190 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.737-3558T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865536 | |||||||
chr6:70865764 | C | T | 3 | a0001c0001t0045g0004 a0001c0002t0042g0253 a0001c0002t0042g0294 |
3 | HG02559.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.737-3786G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865764 | |||||||
chr6:70865784 | A | G | 273 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(270): Show |
276 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.737-3806T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865784 | |||||||
chr6:70865849 | A | C | 11 | a0001c0001t0023g0077 a0001c0001t0023g0078 a0001c0001t0023g0087 others(8): Show |
11 | HG02572.hp1 HG02647.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.737-3871T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865849 | |||||||
chr6:70865869 | G | A | 1 | a0001c0002t0011g0254 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.737-3891C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70865869 | |||||||
chr6:70866006 | G | C | 1 | a0001c0001t0019g0030 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.737-4028C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70866006 | |||||||
chr6:70866165 | G | A | 3 | a0001c0002t0008g0247 a0001c0002t0028g0251 a0001c0002t0098g0292 |
3 | HG02735.hp1 HG02738.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.737-4187C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70866165 | |||||||
chr6:70866349 | A | G | 1 | a0001c0001t0070g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.737-4371T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70866349 | |||||||
chr6:70866439 | A | G | 1 | a0001c0001t0104g0304 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.737-4461T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70866439 | |||||||
chr6:70866566 | G | A | 1 | a0001c0001t0067g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.737-4588C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70866566 | |||||||
chr6:70866626 | T | C | 114 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(111): Show |
116 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.737-4648A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70866626 | |||||||
chr6:70866721 | A | C | 3 | a0001c0001t0045g0004 a0001c0002t0042g0253 a0001c0002t0042g0294 |
3 | HG02559.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.737-4743T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70866721 | |||||||
chr6:70866894 | C | T | 2 | a0001c0001t0023g0087 a0001c0001t0049g0012 |
2 | HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.737-4916G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70866894 | |||||||
chr6:70866911 | T | C | 2 | a0001c0002t0016g0226 a0001c0002t0016g0228 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.737-4933A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70866911 | |||||||
chr6:70866964 | T | C | 1 | a0001c0001t0024g0130 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.737-4986A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70866964 | |||||||
chr6:70867150 | G | A | 1 | a0001c0001t0002g0122 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.737-5172C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70867150 | |||||||
chr6:70867289 | A | G | 22 | a0001c0001t0010g0040 a0001c0001t0010g0052 a0001c0001t0010g0072 others(19): Show |
22 | HG00408.hp2 HG01074.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.737-5311T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70867289 | |||||||
chr6:70867411 | A | C | 7 | a0001c0001t0023g0077 a0001c0001t0023g0078 a0001c0001t0055g0131 others(4): Show |
7 | HG02572.hp1 HG02647.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.737-5433T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70867411 | |||||||
chr6:70867567 | C | A | 2 | a0001c0002t0084g0243 a0002c0004t0063g0175 |
2 | HG01192.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.737-5589G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70867567 | |||||||
chr6:70867653 | T | A | 1 | a0001c0002t0084g0243 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.737-5675A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70867653 | |||||||
chr6:70868100 | C | A | 84 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(81): Show |
86 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.737-6122G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70868100 | |||||||
chr6:70868172 | A | G | 272 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(269): Show |
275 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.737-6194T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70868172 | |||||||
chr6:70868288 | G | T | 1 | a0001c0001t0001g0069 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.737-6310C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70868288 | |||||||
chr6:70868324 | C | T | 1 | a0001c0001t0076g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.737-6346G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70868324 | |||||||
chr6:70868460 | A | G | 1 | a0001c0001t0002g0154 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.737-6482T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70868460 | |||||||
chr6:70868828 | G | C | 1 | a0001c0002t0093g0267 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.737-6850C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70868828 | |||||||
chr6:70868944 | T | A | 1 | a0001c0002t0084g0243 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.737-6966A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70868944 | |||||||
chr6:70869273 | C | T | 72 | a0001c0001t0002g0001 a0001c0001t0002g0035 a0001c0001t0002g0038 others(69): Show |
73 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.737-7295G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70869273 | |||||||
chr6:70869319 | A | G | 125 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(122): Show |
127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.737-7341T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70869319 | |||||||
chr6:70869327 | G | A | 3 | a0001c0001t0045g0004 a0001c0002t0042g0253 a0001c0002t0042g0294 |
3 | HG02559.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.737-7349C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70869327 | |||||||
chr6:70869905 | G | A | 1 | a0001c0001t0012g0026 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.737-7927C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70869905 | |||||||
chr6:70869958 | A | T | 4 | a0001c0001t0024g0041 a0001c0001t0024g0125 a0001c0001t0024g0130 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.737-7980T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70869958 | |||||||
chr6:70869959 | A | C | 4 | a0001c0001t0024g0041 a0001c0001t0024g0125 a0001c0001t0024g0130 others(1): Show |
4 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.737-7981T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70869959 | |||||||
chr6:70869984 | G | A | 1 | a0001c0002t0084g0243 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.737-8006C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70869984 | |||||||
chr6:70870273 | C | A | 44 | a0001c0001t0003g0036 a0001c0001t0003g0081 a0001c0001t0003g0082 others(41): Show |
44 | HG00323.hp2 HG00423.hp1 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.737-8295G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70870273 | |||||||
chr6:70870284 | C | T | 2 | a0001c0002t0084g0243 a0002c0004t0063g0175 |
2 | HG01192.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.737-8306G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70870284 | |||||||
chr6:70870285 | G | A | 2 | a0001c0001t0073g0108 a0001c0002t0096g0260 |
2 | HG02976.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.737-8307C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70870285 | |||||||
chr6:70870307 | C | T | 1 | a0001c0002t0043g0272 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.737-8329G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70870307 | |||||||
chr6:70870433 | C | T | 1 | a0001c0001t0047g0016 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.737-8455G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70870433 | |||||||
chr6:70870631 | A | AAAAC | 11 | a0001c0001t0010g0095 a0001c0001t0010g0124 a0001c0001t0010g0158 others(8): Show |
11 | HG00408.hp2 HG01074.hp1 HG02015.hp1 others(8): Show |
intron_variant | MODIFIER | c.737-8657_737-8654d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70870631 | |||||||
chr6:70870840 | C | T | 1 | a0001c0002t0006g0193 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.737-8862G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70870840 | |||||||
chr6:70871050 | T | C | 15 | a0001c0001t0010g0095 a0001c0001t0010g0124 a0001c0001t0010g0158 others(12): Show |
15 | HG00408.hp2 HG01074.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.737-9072A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871050 | |||||||
chr6:70871108 | A | G | 2 | a0001c0002t0084g0243 a0002c0004t0063g0175 |
2 | HG01192.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.737-9130T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871108 | |||||||
chr6:70871154 | AT | A | 51 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(48): Show |
52 | HG00099.hp2 HG00544.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.737-9177delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871154 | |||||||
chr6:70871215 | TTTTTTTG | T | 17 | a0001c0001t0001g0144 a0001c0001t0001g0157 a0001c0001t0009g0084 others(14): Show |
17 | HG01069.hp1 HG01975.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.737-9244_737-9238d others(9): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871215 | |||||||
chr6:70871216 | TTTTTTG | T | 70 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(67): Show |
72 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.737-9244_737-9239d others(8): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871216 | |||||||
chr6:70871217 | TTTTTG | T | 16 | a0001c0001t0001g0061 a0001c0001t0010g0124 a0001c0001t0010g0158 others(13): Show |
16 | HG00408.hp2 HG01074.hp1 HG02027.hp2 others(13): Show |
intron_variant | MODIFIER | c.737-9244_737-9240d others(7): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871217 | |||||||
chr6:70871220 | TTG | T | 6 | a0001c0001t0045g0004 a0001c0001t0055g0131 a0001c0001t0069g0104 others(3): Show |
6 | HG02559.hp1 HG02717.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.737-9244_737-9243d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871220 | |||||||
chr6:70871221 | TG | T | 5 | a0001c0001t0023g0087 a0001c0001t0049g0012 a0001c0001t0066g0143 others(2): Show |
5 | HG02572.hp1 HG02647.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.737-9244delC | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871221 | |||||||
chr6:70871222 | G | T | 2 | a0001c0001t0002g0051 a0001c0001t0032g0005 |
2 | NA18940.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.737-9244C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871222 | |||||||
chr6:70871222 | GT | G | 69 | a0001c0001t0002g0001 a0001c0001t0002g0035 a0001c0001t0002g0038 others(66): Show |
70 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.737-9245delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871222 | |||||||
chr6:70871223 | T | G | 2 | a0001c0001t0002g0051 a0001c0001t0032g0005 |
2 | NA18940.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.737-9245A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871223 | |||||||
chr6:70871227 | T | G | 1 | a0001c0002t0016g0205 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.737-9249A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871227 | |||||||
chr6:70871441 | C | T | 2 | a0001c0001t0023g0087 a0001c0001t0049g0012 |
2 | HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.737-9463G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871441 | |||||||
chr6:70871680 | G | T | 115 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(112): Show |
117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.737-9702C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871680 | |||||||
chr6:70871937 | T | C | 105 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(102): Show |
107 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.737-9959A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871937 | |||||||
chr6:70871989 | T | C | 1 | a0001c0003t0062g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.737-10011A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70871989 | |||||||
chr6:70872037 | C | T | 86 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(83): Show |
88 | HG00099.hp2 HG00323.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.737-10059G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70872037 | |||||||
chr6:70872160 | C | T | 1 | a0002c0004t0063g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.737-10182G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70872160 | |||||||
chr6:70872161 | G | A | 5 | a0001c0001t0025g0110 a0001c0001t0025g0111 a0001c0001t0025g0138 others(2): Show |
5 | HG01069.hp1 HG02809.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.737-10183C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70872161 | |||||||
chr6:70872190 | T | C | 2 | a0001c0001t0023g0087 a0001c0001t0049g0012 |
2 | HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.737-10212A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70872190 | |||||||
chr6:70872459 | G | A | 1 | a0001c0001t0070g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.737-10481C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70872459 | |||||||
chr6:70872504 | CT | C | 19 | a0001c0001t0002g0066 a0001c0001t0023g0077 a0001c0001t0023g0078 others(16): Show |
19 | HG01192.hp1 HG02559.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.737-10527delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70872504 | |||||||
chr6:70872504 | CTT | C | 99 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(96): Show |
101 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.737-10528_737-1052 others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70872504 | |||||||
chr6:70872522 | G | T | 2 | a0001c0002t0014g0283 a0001c0002t0095g0282 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.737-10544C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70872522 | |||||||
chr6:70872729 | T | C | 6 | a0001c0001t0003g0082 a0001c0001t0003g0136 a0001c0001t0003g0137 others(3): Show |
6 | HG01884.hp2 HG02280.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.737-10751A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70872729 | |||||||
chr6:70872986 | T | G | 113 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(110): Show |
115 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.737-11008A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70872986 | |||||||
chr6:70873019 | C | A | 1 | a0001c0001t0069g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.737-11041G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873019 | |||||||
chr6:70873174 | C | G | 115 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(112): Show |
117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.737-11196G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873174 | |||||||
chr6:70873176 | G | A | 1 | a0001c0001t0002g0059 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.737-11198C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873176 | |||||||
chr6:70873311 | A | G | 6 | a0001c0001t0023g0087 a0001c0001t0049g0012 a0001c0001t0055g0131 others(3): Show |
6 | HG02572.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.737-11333T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873311 | |||||||
chr6:70873497 | T | G | 2 | a0001c0001t0004g0099 a0001c0002t0040g0222 |
2 | HG00323.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.737-11519A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873497 | |||||||
chr6:70873604 | T | C | 1 | a0001c0001t0069g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.737-11626A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873604 | |||||||
chr6:70873672 | C | T | 2 | a0001c0002t0014g0288 a0001c0002t0027g0219 |
2 | HG00642.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.737-11694G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873672 | |||||||
chr6:70873735 | G | A | 58 | a0001c0001t0001g0161 a0001c0001t0002g0001 a0001c0001t0002g0035 others(55): Show |
59 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.737-11757C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873735 | |||||||
chr6:70873762 | G | A | 1 | a0001c0001t0001g0102 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.737-11784C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873762 | |||||||
chr6:70873896 | A | T | 125 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(122): Show |
127 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.737-11918T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873896 | |||||||
chr6:70873945 | C | T | 1 | a0001c0001t0069g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.737-11967G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70873945 | |||||||
chr6:70874101 | C | T | 111 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(108): Show |
113 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.737-12123G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70874101 | |||||||
chr6:70874243 | CCTTGAAC others(3): Show |
C | 4 | a0001c0001t0055g0131 a0001c0001t0066g0143 a0001c0002t0041g0196 others(1): Show |
4 | HG02572.hp1 HG02647.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.737-12275_737-1226 others(14): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70874243 | |||||||
chr6:70874609 | A | G | 2 | a0001c0001t0023g0087 a0001c0001t0049g0012 |
2 | HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.737-12631T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70874609 | |||||||
chr6:70874733 | A | G | 4 | a0001c0001t0036g0105 a0001c0001t0036g0142 a0001c0002t0100g0256 others(1): Show |
4 | HG02109.hp2 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.737-12755T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70874733 | |||||||
chr6:70874871 | A | G | 3 | a0001c0001t0012g0023 a0001c0001t0012g0028 a0001c0002t0039g0246 |
3 | HG02027.hp1 HG02155.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.737-12893T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70874871 | |||||||
chr6:70874998 | C | CT | 5 | a0001c0001t0025g0110 a0001c0001t0025g0111 a0001c0001t0025g0138 others(2): Show |
5 | HG01069.hp1 HG02809.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.737-13021dupA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70874998 | |||||||
chr6:70875004 | T | A | 3 | a0001c0001t0045g0004 a0001c0002t0042g0253 a0001c0002t0042g0294 |
3 | HG02559.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.737-13026A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875004 | |||||||
chr6:70875005 | A | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(99): Show |
104 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.737-13027T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875005 | |||||||
chr6:70875006 | A | T | 26 | a0001c0001t0009g0093 a0001c0001t0010g0095 a0001c0001t0020g0054 others(23): Show |
27 | HG00323.hp1 HG00735.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.737-13028T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875006 | |||||||
chr6:70875104 | C | A | 9 | a0001c0001t0003g0103 a0001c0001t0003g0127 a0001c0001t0003g0134 others(6): Show |
9 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.737-13126G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875104 | |||||||
chr6:70875192 | C | T | 3 | a0001c0001t0045g0004 a0001c0002t0042g0253 a0001c0002t0042g0294 |
3 | HG02559.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.737-13214G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875192 | |||||||
chr6:70875226 | TGTAATGT others(3): Show |
T | 9 | a0001c0001t0013g0086 a0001c0001t0013g0129 a0001c0001t0017g0008 others(6): Show |
9 | HG01255.hp1 HG01952.hp2 HG01978.hp2 others(6): Show |
intron_variant | MODIFIER | c.737-13258_737-1324 others(14): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875226 | |||||||
chr6:70875290 | C | A | 1 | a0001c0001t0003g0169 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.737-13312G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875290 | |||||||
chr6:70875306 | C | T | 4 | a0001c0001t0036g0105 a0001c0001t0036g0142 a0001c0002t0100g0256 others(1): Show |
4 | HG02109.hp2 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.737-13328G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875306 | |||||||
chr6:70875348 | G | A | 15 | a0001c0001t0010g0095 a0001c0001t0010g0124 a0001c0001t0010g0158 others(12): Show |
15 | HG00408.hp2 HG01074.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.737-13370C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875348 | |||||||
chr6:70875381 | T | A | 1 | a0001c0001t0070g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.737-13403A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875381 | |||||||
chr6:70875436 | C | A | 2 | a0001c0001t0003g0081 a0001c0001t0003g0169 |
2 | HG03490.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.737-13458G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875436 | |||||||
chr6:70875513 | C | T | 1 | a0001c0002t0015g0277 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.737-13535G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875513 | |||||||
chr6:70875801 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.737-13823C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875801 | |||||||
chr6:70875887 | C | A | 15 | a0001c0001t0010g0095 a0001c0001t0010g0124 a0001c0001t0010g0158 others(12): Show |
15 | HG00408.hp2 HG01074.hp1 HG02015.hp1 others(12): Show |
intron_variant | MODIFIER | c.737-13909G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875887 | |||||||
chr6:70875978 | G | C | 3 | a0001c0001t0045g0004 a0001c0002t0042g0253 a0001c0002t0042g0294 |
3 | HG02559.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.737-14000C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70875978 | |||||||
chr6:70876118 | T | A | 1 | a0001c0001t0001g0069 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.737-14140A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70876118 | |||||||
chr6:70876444 | A | T | 2 | a0001c0002t0021g0182 a0001c0002t0038g0179 |
2 | NA19056.hp1 NA19070.hp2 |
intron_variant | MODIFIER | c.737-14466T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70876444 | |||||||
chr6:70876549 | C | T | 1 | a0001c0001t0070g0112 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.737-14571G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70876549 | |||||||
chr6:70876670 | T | C | 8 | a0001c0001t0023g0087 a0001c0001t0049g0012 a0001c0001t0055g0131 others(5): Show |
8 | HG02572.hp1 HG02647.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.737-14692A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70876670 | |||||||
chr6:70877021 | A | T | 1 | a0001c0002t0031g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.737-15043T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70877021 | |||||||
chr6:70877026 | G | A | 1 | a0001c0001t0003g0100 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.737-15048C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70877026 | |||||||
chr6:70877239 | C | G | 1 | a0001c0002t0015g0252 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.737-15261G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70877239 | |||||||
chr6:70877301 | A | G | 1 | a0001c0002t0005g0214 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.737-15323T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70877301 | |||||||
chr6:70877898 | C | T | 1 | a0001c0001t0003g0137 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.737-15920G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70877898 | |||||||
chr6:70877911 | C | A | 1 | a0001c0002t0014g0291 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.737-15933G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70877911 | |||||||
chr6:70878331 | T | G | 1 | a0001c0002t0006g0234 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.736+15797A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878331 | |||||||
chr6:70878458 | G | A | 22 | a0001c0001t0010g0040 a0001c0001t0010g0052 a0001c0001t0010g0072 others(19): Show |
22 | HG00408.hp2 HG01074.hp1 HG01099.hp2 others(19): Show |
intron_variant | MODIFIER | c.736+15670C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878458 | |||||||
chr6:70878480 | T | C | 1 | a0001c0001t0045g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.736+15648A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878480 | |||||||
chr6:70878506 | TATAGTTT others(26): Show |
T | 1 | a0001c0001t0013g0129 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.736+15589_736+1562 others(37): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878506 | |||||||
chr6:70878612 | C | A | 2 | a0001c0001t0023g0087 a0001c0001t0049g0012 |
2 | HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.736+15516G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878612 | |||||||
chr6:70878681 | C | T | 3 | a0001c0001t0020g0079 a0001c0002t0015g0280 a0001c0002t0028g0221 |
3 | HG00323.hp1 HG02886.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.736+15447G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878681 | |||||||
chr6:70878802 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.736+15326C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878802 | |||||||
chr6:70878874 | C | T | 2 | a0001c0002t0005g0232 a0001c0002t0005g0233 |
2 | NA18960.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.736+15254G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878874 | |||||||
chr6:70878878 | T | C | 2 | a0001c0001t0023g0087 a0001c0001t0049g0012 |
2 | HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.736+15250A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878878 | |||||||
chr6:70878917 | A | G | 1 | a0001c0001t0001g0061 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.736+15211T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878917 | |||||||
chr6:70878957 | G | C | 115 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(112): Show |
117 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.736+15171C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878957 | |||||||
chr6:70878969 | C | T | 2 | a0001c0001t0002g0150 a0001c0001t0071g0039 |
2 | NA18945.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.736+15159G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70878969 | |||||||
chr6:70879043 | C | T | 3 | a0001c0001t0045g0004 a0001c0002t0042g0253 a0001c0002t0042g0294 |
3 | HG02559.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.736+15085G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879043 | |||||||
chr6:70879103 | C | T | 113 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(110): Show |
115 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.736+15025G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879103 | |||||||
chr6:70879158 | G | T | 6 | a0001c0001t0023g0087 a0001c0001t0049g0012 a0001c0001t0055g0131 others(3): Show |
6 | HG02572.hp1 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.736+14970C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879158 | |||||||
chr6:70879189 | T | TTTG | 109 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(106): Show |
111 | HG00099.hp2 HG00323.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.736+14936_736+1493 others(7): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879189 | |||||||
chr6:70879434 | G | A | 1 | a0001c0001t0012g0028 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.736+14694C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879434 | |||||||
chr6:70879480 | G | GATTCATT others(1): Show |
10 | a0001c0001t0002g0070 a0001c0001t0012g0031 a0001c0001t0023g0077 others(7): Show |
10 | HG00423.hp2 HG00673.hp2 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.736+14640_736+1464 others(12): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879480 | |||||||
chr6:70879480 | G | GATTCATT others(5): Show |
16 | a0001c0001t0002g0066 a0001c0001t0002g0122 a0001c0001t0002g0152 others(13): Show |
16 | HG00544.hp1 HG01884.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.736+14636_736+1464 others(16): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879480 | |||||||
chr6:70879480 | G | GATTCATT others(9): Show |
45 | a0001c0001t0002g0001 a0001c0001t0002g0035 a0001c0001t0002g0038 others(42): Show |
46 | HG00099.hp1 HG00408.hp1 HG01192.hp1 others(43): Show |
intron_variant | MODIFIER | c.736+14632_736+1464 others(20): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879480 | |||||||
chr6:70879480 | G | GATTCATT others(13): Show |
2 | a0001c0001t0004g0053 a0001c0002t0092g0264 |
2 | NA18951.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.736+14628_736+1464 others(24): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879480 | |||||||
chr6:70879505 | A | C | 1 | a0001c0002t0096g0260 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.736+14623T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879505 | |||||||
chr6:70879514 | A | C | 1 | a0001c0001t0002g0060 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.736+14614T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879514 | |||||||
chr6:70879517 | C | T | 12 | a0001c0001t0002g0051 a0001c0001t0002g0071 a0001c0001t0002g0152 others(9): Show |
12 | HG02040.hp1 HG02135.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.736+14611G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879517 | |||||||
chr6:70879806 | G | A | 23 | a0001c0001t0010g0052 a0001c0001t0010g0072 a0001c0001t0010g0085 others(20): Show |
23 | HG00408.hp2 HG01074.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.736+14322C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879806 | |||||||
chr6:70879819 | C | T | 1 | a0001c0001t0072g0037 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.736+14309G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879819 | |||||||
chr6:70879874 | G | A | 4 | a0001c0001t0036g0105 a0001c0001t0036g0142 a0001c0002t0100g0256 others(1): Show |
4 | HG02109.hp2 HG02647.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.736+14254C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879874 | |||||||
chr6:70879898 | G | A | 26 | a0001c0001t0004g0141 a0001c0001t0010g0052 a0001c0001t0010g0072 others(23): Show |
26 | HG00408.hp2 HG01074.hp1 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.736+14230C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879898 | |||||||
chr6:70879918 | T | C | 9 | a0001c0001t0002g0001 a0001c0001t0002g0038 a0001c0001t0002g0043 others(6): Show |
10 | HG00423.hp2 HG02015.hp2 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.736+14210A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879918 | |||||||
chr6:70879991 | G | A | 1 | a0001c0001t0069g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.736+14137C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70879991 | |||||||
chr6:70880079 | C | CGTGGGGG others(5): Show |
1 | a0001c0003t0062g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.736+14037_736+1404 others(16): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70880079 | |||||||
chr6:70880478 | A | C | 5 | a0001c0001t0023g0087 a0001c0001t0037g0062 a0001c0001t0037g0089 others(2): Show |
5 | HG02723.hp2 HG03239.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.736+13650T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70880478 | |||||||
chr6:70880507 | T | C | 1 | a0002c0004t0063g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.736+13621A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70880507 | |||||||
chr6:70880654 | A | AT | 9 | a0001c0001t0002g0001 a0001c0001t0002g0043 a0001c0001t0023g0087 others(6): Show |
10 | HG02572.hp1 HG02723.hp2 HG03239.hp1 others(7): Show |
intron_variant | MODIFIER | c.736+13473dupA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70880654 | |||||||
chr6:70880921 | C | T | 1 | a0001c0002t0043g0272 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.736+13207G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70880921 | |||||||
chr6:70880986 | T | G | 1 | a0001c0001t0013g0129 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.736+13142A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70880986 | |||||||
chr6:70881000 | A | T | 1 | a0001c0001t0013g0129 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.736+13128T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70881000 | |||||||
chr6:70881368 | A | G | 2 | a0001c0001t0004g0141 a0001c0002t0080g0194 |
2 | HG02572.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.736+12760T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70881368 | |||||||
chr6:70881507 | T | C | 1 | a0001c0002t0027g0212 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.736+12621A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70881507 | |||||||
chr6:70881521 | G | A | 1 | a0001c0001t0010g0158 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.736+12607C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70881521 | |||||||
chr6:70881563 | C | T | 1 | a0001c0001t0061g0094 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.736+12565G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70881563 | |||||||
chr6:70881574 | C | G | 92 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0047 others(89): Show |
94 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.736+12554G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70881574 | |||||||
chr6:70881686 | G | A | 6 | a0001c0001t0004g0140 a0001c0001t0023g0087 a0001c0001t0037g0062 others(3): Show |
6 | HG02723.hp2 HG03239.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.736+12442C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70881686 | |||||||
chr6:70881734 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.736+12394C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70881734 | |||||||
chr6:70881838 | C | T | 1 | a0001c0002t0006g0187 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.736+12290G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70881838 | |||||||
chr6:70881921 | C | T | 1 | a0001c0001t0003g0082 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.736+12207G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70881921 | |||||||
chr6:70882154 | T | C | 1 | a0001c0001t0004g0053 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.736+11974A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882154 | |||||||
chr6:70882199 | C | T | 1 | a0001c0002t0011g0270 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.736+11929G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882199 | |||||||
chr6:70882220 | C | T | 5 | a0001c0001t0004g0141 a0001c0001t0068g0168 a0001c0002t0042g0253 others(2): Show |
5 | HG02572.hp1 HG03098.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.736+11908G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882220 | |||||||
chr6:70882229 | T | C | 1 | a0001c0001t0003g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.736+11899A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882229 | |||||||
chr6:70882277 | A | G | 1 | a0001c0001t0068g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.736+11851T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882277 | |||||||
chr6:70882298 | C | G | 1 | a0001c0002t0011g0269 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.736+11830G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882298 | |||||||
chr6:70882306 | A | C | 2 | a0001c0002t0011g0255 a0001c0002t0094g0274 |
2 | HG00099.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.736+11822T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882306 | |||||||
chr6:70882379 | T | C | 1 | a0001c0002t0021g0237 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.736+11749A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882379 | |||||||
chr6:70882425 | C | T | 1 | a0001c0001t0076g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.736+11703G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882425 | |||||||
chr6:70882502 | A | G | 6 | a0001c0001t0004g0140 a0001c0001t0023g0087 a0001c0001t0037g0062 others(3): Show |
6 | HG02723.hp2 HG03239.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.736+11626T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882502 | |||||||
chr6:70882504 | A | C | 3 | a0001c0001t0066g0143 a0001c0002t0041g0196 a0001c0002t0043g0272 |
3 | HG02647.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.736+11624T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882504 | |||||||
chr6:70882785 | A | G | 5 | a0001c0001t0023g0087 a0001c0001t0037g0062 a0001c0001t0037g0089 others(2): Show |
5 | HG02723.hp2 HG03239.hp1 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.736+11343T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882785 | |||||||
chr6:70882923 | AATGT | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0047 others(72): Show |
77 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.736+11201_736+1120 others(8): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70882923 | |||||||
chr6:70883124 | G | A | 75 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0047 others(72): Show |
77 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.736+11004C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883124 | |||||||
chr6:70883351 | C | T | 1 | a0001c0002t0043g0272 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.736+10777G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883351 | |||||||
chr6:70883444 | T | C | 1 | a0002c0004t0063g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.736+10684A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883444 | |||||||
chr6:70883460 | C | CA | 12 | a0001c0001t0036g0105 a0001c0001t0036g0142 a0001c0001t0066g0143 others(9): Show |
12 | HG00642.hp2 HG01496.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.736+10667dupT | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883460 | |||||||
chr6:70883460 | CA | C | 77 | a0001c0001t0002g0066 a0001c0001t0002g0070 a0001c0001t0003g0082 others(74): Show |
77 | HG00408.hp2 HG00423.hp1 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.736+10667delT | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883460 | |||||||
chr6:70883475 | A | G | 1 | a0001c0001t0045g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.736+10653T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883475 | |||||||
chr6:70883503 | G | A | 1 | a0002c0004t0063g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.736+10625C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883503 | |||||||
chr6:70883621 | G | A | 3 | a0001c0001t0003g0103 a0001c0001t0003g0127 a0001c0001t0004g0126 |
3 | HG00741.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.736+10507C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883621 | |||||||
chr6:70883649 | A | G | 5 | a0001c0001t0025g0110 a0001c0001t0025g0111 a0001c0001t0025g0138 others(2): Show |
5 | HG01069.hp1 HG02809.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.736+10479T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883649 | |||||||
chr6:70883703 | A | G | 1 | a0001c0002t0005g0232 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.736+10425T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883703 | |||||||
chr6:70883730 | C | T | 5 | a0001c0001t0036g0105 a0001c0001t0036g0142 a0001c0002t0100g0256 others(2): Show |
5 | HG02109.hp2 HG02647.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.736+10398G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883730 | |||||||
chr6:70883793 | T | C | 1 | a0001c0001t0044g0305 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.736+10335A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883793 | |||||||
chr6:70883949 | C | T | 1 | a0001c0002t0041g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.736+10179G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70883949 | |||||||
chr6:70884016 | G | A | 1 | a0001c0001t0003g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.736+10112C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884016 | |||||||
chr6:70884095 | C | CA | 10 | a0001c0001t0001g0064 a0001c0001t0001g0065 a0001c0001t0001g0119 others(7): Show |
10 | HG00621.hp2 HG00735.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.736+10032dupT | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884095 | |||||||
chr6:70884095 | CA | C | 189 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0002g0001 others(186): Show |
190 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.736+10032delT | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884095 | |||||||
chr6:70884100 | AAAAAAAA others(7): Show |
A | 1 | a0001c0001t0004g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.736+10014_736+1002 others(18): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884100 | |||||||
chr6:70884102 | A | C | 4 | a0001c0001t0055g0131 a0001c0001t0066g0143 a0001c0002t0041g0196 others(1): Show |
4 | HG02647.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.736+10026T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884102 | |||||||
chr6:70884103 | AAAAAAAA others(4): Show |
A | 4 | a0001c0001t0023g0087 a0001c0001t0037g0062 a0001c0001t0037g0089 others(1): Show |
4 | HG02723.hp2 HG03239.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.736+10014_736+1002 others(15): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884103 | |||||||
chr6:70884104 | AAAAAAAA others(3): Show |
A | 1 | a0001c0001t0074g0088 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.736+10014_736+1002 others(14): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884104 | |||||||
chr6:70884108 | A | C | 4 | a0001c0001t0055g0131 a0001c0001t0066g0143 a0001c0002t0041g0196 others(1): Show |
4 | HG02647.hp1 HG03195.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.736+10020T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884108 | |||||||
chr6:70884113 | A | C | 2 | a0001c0001t0004g0109 a0001c0002t0077g0178 |
2 | HG02486.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.736+10015T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884113 | |||||||
chr6:70884114 | C | A | 4 | a0001c0001t0002g0073 a0001c0001t0004g0109 a0001c0001t0034g0107 others(1): Show |
4 | HG02486.hp2 HG02818.hp2 NA18967.hp2 others(1): Show |
intron_variant | MODIFIER | c.736+10014G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884114 | |||||||
chr6:70884142 | C | T | 1 | a0001c0002t0028g0221 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.736+9986G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884142 | |||||||
chr6:70884171 | T | A | 1 | a0001c0001t0068g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.736+9957A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884171 | |||||||
chr6:70884175 | T | A | 1 | a0001c0001t0068g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.736+9953A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884175 | |||||||
chr6:70884179 | C | T | 1 | a0001c0002t0011g0270 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.736+9949G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884179 | |||||||
chr6:70884203 | G | A | 9 | a0001c0001t0010g0052 a0001c0001t0010g0072 a0001c0001t0010g0085 others(6): Show |
9 | HG01099.hp2 HG01261.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.736+9925C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884203 | |||||||
chr6:70884263 | C | G | 1 | a0001c0001t0045g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.736+9865G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884263 | |||||||
chr6:70884507 | C | G | 155 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(152): Show |
158 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.736+9621G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884507 | |||||||
chr6:70884580 | A | G | 1 | a0001c0002t0008g0220 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.736+9548T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70884580 | |||||||
chr6:70885059 | C | T | 68 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0047 others(65): Show |
70 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(67): Show |
intron_variant | MODIFIER | c.736+9069G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885059 | |||||||
chr6:70885082 | A | C | 158 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0002g0001 others(155): Show |
159 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.736+9046T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885082 | |||||||
chr6:70885342 | G | A | 5 | a0001c0001t0025g0110 a0001c0001t0025g0111 a0001c0001t0025g0138 others(2): Show |
5 | HG01069.hp1 HG02809.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.736+8786C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885342 | |||||||
chr6:70885372 | T | G | 157 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0002g0001 others(154): Show |
158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.736+8756A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885372 | |||||||
chr6:70885405 | T | A | 1 | a0001c0001t0004g0141 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.736+8723A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885405 | |||||||
chr6:70885448 | T | C | 157 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0002g0001 others(154): Show |
158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.736+8680A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885448 | |||||||
chr6:70885618 | G | A | 157 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0002g0001 others(154): Show |
158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.736+8510C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885618 | |||||||
chr6:70885645 | G | A | 2 | a0001c0001t0019g0030 a0001c0002t0021g0237 |
2 | HG02027.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.736+8483C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885645 | |||||||
chr6:70885687 | A | T | 1 | a0001c0002t0091g0259 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.736+8441T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885687 | |||||||
chr6:70885723 | C | A | 1 | a0001c0001t0104g0304 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.736+8405G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885723 | |||||||
chr6:70885779 | C | T | 1 | a0002c0004t0063g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.736+8349G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885779 | |||||||
chr6:70885868 | T | G | 76 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0047 others(73): Show |
78 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.736+8260A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885868 | |||||||
chr6:70885886 | A | G | 157 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0002g0001 others(154): Show |
158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.736+8242T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885886 | |||||||
chr6:70885922 | A | G | 4 | a0001c0001t0003g0145 a0001c0001t0003g0146 a0001c0001t0003g0147 others(1): Show |
4 | HG00423.hp1 HG02129.hp1 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.736+8206T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885922 | |||||||
chr6:70885941 | T | G | 2 | a0001c0001t0037g0089 a0001c0001t0074g0088 |
2 | HG03669.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.736+8187A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885941 | |||||||
chr6:70885945 | C | G | 157 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0002g0001 others(154): Show |
158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.736+8183G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70885945 | |||||||
chr6:70886013 | G | A | 1 | a0001c0001t0045g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.736+8115C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886013 | |||||||
chr6:70886044 | G | C | 1 | a0002c0004t0063g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.736+8084C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886044 | |||||||
chr6:70886095 | A | G | 22 | a0001c0001t0001g0144 a0001c0001t0004g0053 a0001c0001t0004g0057 others(19): Show |
22 | HG00408.hp2 HG01884.hp1 HG02258.hp2 others(19): Show |
intron_variant | MODIFIER | c.736+8033T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886095 | |||||||
chr6:70886221 | A | G | 157 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0002g0001 others(154): Show |
158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.736+7907T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886221 | |||||||
chr6:70886325 | G | A | 157 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0002g0001 others(154): Show |
158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.736+7803C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886325 | |||||||
chr6:70886423 | T | C | 157 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0002g0001 others(154): Show |
158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.736+7705A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886423 | |||||||
chr6:70886513 | T | A | 1 | a0001c0001t0067g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.736+7615A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886513 | |||||||
chr6:70886560 | G | C | 157 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0002g0001 others(154): Show |
158 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.736+7568C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886560 | |||||||
chr6:70886581 | C | T | 1 | a0001c0001t0002g0066 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.736+7547G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886581 | |||||||
chr6:70886660 | C | T | 1 | a0002c0004t0063g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.736+7468G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886660 | |||||||
chr6:70886768 | G | C | 1 | a0001c0001t0009g0048 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.736+7360C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886768 | |||||||
chr6:70886782 | CCTGCAAG others(8): Show |
C | 1 | a0001c0001t0002g0073 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.736+7331_736+7345d others(17): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886782 | |||||||
chr6:70886983 | C | T | 155 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0002g0001 others(152): Show |
156 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.736+7145G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886983 | |||||||
chr6:70886992 | G | C | 155 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0002g0001 others(152): Show |
156 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(153): Show |
intron_variant | MODIFIER | c.736+7136C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70886992 | |||||||
chr6:70887037 | G | C | 233 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(230): Show |
236 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.736+7091C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887037 | |||||||
chr6:70887350 | C | T | 154 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0002g0001 others(151): Show |
155 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.736+6778G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887350 | |||||||
chr6:70887379 | C | G | 156 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0002g0001 others(153): Show |
157 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.736+6749G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887379 | |||||||
chr6:70887466 | A | T | 7 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0036g0105 others(4): Show |
7 | HG02109.hp2 HG02630.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.736+6662T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887466 | |||||||
chr6:70887485 | C | T | 1 | a0001c0001t0003g0101 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.736+6643G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887485 | |||||||
chr6:70887563 | G | T | 153 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0002g0001 others(150): Show |
154 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.736+6565C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887563 | |||||||
chr6:70887628 | G | A | 154 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0002g0001 others(151): Show |
155 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.736+6500C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887628 | |||||||
chr6:70887674 | G | T | 1 | a0002c0004t0063g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.736+6454C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887674 | |||||||
chr6:70887688 | G | C | 75 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0047 others(72): Show |
77 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.736+6440C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887688 | |||||||
chr6:70887711 | T | C | 6 | a0001c0001t0004g0141 a0001c0001t0023g0087 a0001c0001t0037g0062 others(3): Show |
6 | HG02723.hp2 HG03130.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.736+6417A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887711 | |||||||
chr6:70887861 | A | G | 3 | a0001c0001t0068g0168 a0001c0002t0042g0253 a0001c0002t0042g0294 |
3 | HG03098.hp1 HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.736+6267T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70887861 | |||||||
chr6:70888115 | C | T | 67 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0002g0001 others(64): Show |
68 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(65): Show |
intron_variant | MODIFIER | c.736+6013G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888115 | |||||||
chr6:70888125 | C | T | 140 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0002g0001 others(137): Show |
141 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.736+6003G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888125 | |||||||
chr6:70888207 | T | C | 1 | a0001c0003t0062g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.736+5921A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888207 | |||||||
chr6:70888224 | AT | A | 77 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0002g0001 others(74): Show |
78 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(75): Show |
intron_variant | MODIFIER | c.736+5903delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888224 | |||||||
chr6:70888288 | G | C | 1 | a0001c0002t0006g0188 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.736+5840C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888288 | |||||||
chr6:70888359 | C | T | 8 | a0001c0001t0004g0141 a0001c0001t0023g0077 a0001c0001t0023g0078 others(5): Show |
8 | HG02723.hp2 HG03130.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.736+5769G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888359 | |||||||
chr6:70888378 | A | C | 9 | a0001c0001t0004g0140 a0001c0001t0004g0141 a0001c0001t0023g0077 others(6): Show |
9 | HG02723.hp2 HG03130.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.736+5750T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888378 | |||||||
chr6:70888470 | G | C | 8 | a0001c0001t0004g0141 a0001c0001t0023g0077 a0001c0001t0023g0078 others(5): Show |
8 | HG02723.hp2 HG03130.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.736+5658C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888470 | |||||||
chr6:70888493 | AG | A | 3 | a0001c0001t0066g0143 a0001c0002t0041g0196 a0001c0002t0043g0272 |
3 | HG02647.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.736+5634delC | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888493 | |||||||
chr6:70888505 | C | G | 9 | a0001c0001t0004g0140 a0001c0001t0004g0141 a0001c0001t0023g0077 others(6): Show |
9 | HG02723.hp2 HG03130.hp2 HG03139.hp2 others(6): Show |
intron_variant | MODIFIER | c.736+5623G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888505 | |||||||
chr6:70888546 | G | C | 68 | a0001c0001t0002g0066 a0001c0001t0002g0070 a0001c0001t0003g0082 others(65): Show |
68 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.736+5582C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888546 | |||||||
chr6:70888599 | A | G | 1 | a0001c0001t0055g0131 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.736+5529T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888599 | |||||||
chr6:70888664 | G | A | 22 | a0001c0001t0019g0018 a0001c0001t0019g0030 a0001c0001t0020g0054 others(19): Show |
22 | HG00323.hp1 HG01074.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.736+5464C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888664 | |||||||
chr6:70888736 | T | G | 1 | a0001c0002t0005g0232 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.736+5392A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888736 | |||||||
chr6:70888842 | C | T | 152 | a0001c0001t0001g0042 a0001c0001t0001g0144 a0001c0001t0002g0001 others(149): Show |
153 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.736+5286G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888842 | |||||||
chr6:70888868 | C | T | 79 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0047 others(76): Show |
81 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(78): Show |
intron_variant | MODIFIER | c.736+5260G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888868 | |||||||
chr6:70888885 | C | T | 1 | a0001c0001t0054g0032 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.736+5243G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888885 | |||||||
chr6:70888921 | T | C | 3 | a0001c0001t0003g0103 a0001c0001t0003g0127 a0001c0001t0004g0126 |
3 | HG00741.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.736+5207A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888921 | |||||||
chr6:70888956 | G | C | 6 | a0001c0001t0017g0019 a0001c0001t0020g0098 a0001c0002t0008g0003 others(3): Show |
7 | HG00735.hp2 HG00738.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.736+5172C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888956 | |||||||
chr6:70888957 | A | G | 1 | a0001c0001t0045g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.736+5171T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70888957 | |||||||
chr6:70889064 | A | C | 20 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0003g0100 others(17): Show |
20 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(17): Show |
intron_variant | MODIFIER | c.736+5064T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889064 | |||||||
chr6:70889294 | ATTAAAGA others(2671): Show |
A | 1 | a0001c0001t0068g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.736+2156_736+4833d others(2): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889294 | |||||||
chr6:70889439 | C | G | 3 | a0001c0001t0066g0143 a0001c0002t0041g0196 a0001c0002t0043g0272 |
3 | HG02647.hp1 HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.736+4689G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889439 | |||||||
chr6:70889487 | C | T | 1 | a0001c0002t0005g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.736+4641G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889487 | |||||||
chr6:70889517 | C | T | 5 | a0001c0001t0018g0007 a0001c0001t0051g0006 a0001c0002t0007g0213 others(2): Show |
5 | HG02280.hp1 HG02451.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.736+4611G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889517 | |||||||
chr6:70889615 | C | T | 46 | a0001c0001t0002g0066 a0001c0001t0002g0070 a0001c0001t0003g0082 others(43): Show |
46 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.736+4513G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889615 | |||||||
chr6:70889617 | C | T | 1 | a0001c0001t0105g0306 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.736+4511G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889617 | |||||||
chr6:70889716 | C | T | 43 | a0001c0001t0001g0042 a0001c0001t0002g0001 a0001c0001t0002g0035 others(40): Show |
44 | HG00408.hp1 HG02015.hp2 HG02027.hp1 others(41): Show |
intron_variant | MODIFIER | c.736+4412G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889716 | |||||||
chr6:70889764 | C | G | 3 | a0001c0001t0060g0120 a0001c0002t0006g0245 a0001c0002t0016g0244 |
3 | HG02165.hp2 HG03831.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.736+4364G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889764 | |||||||
chr6:70889786 | A | AT | 6 | a0001c0001t0003g0139 a0001c0001t0004g0109 a0001c0001t0034g0107 others(3): Show |
6 | HG01884.hp1 HG02486.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.736+4341dupA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889786 | |||||||
chr6:70889786 | AT | A | 94 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0047 others(91): Show |
95 | HG00099.hp2 HG00323.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.736+4341delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889786 | |||||||
chr6:70889787 | T | C | 1 | a0001c0001t0108g0312 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.736+4341A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889787 | |||||||
chr6:70889803 | G | T | 1 | a0001c0001t0073g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.736+4325C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889803 | |||||||
chr6:70889839 | G | C | 1 | a0001c0001t0055g0131 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.736+4289C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889839 | |||||||
chr6:70889852 | G | A | 1 | a0001c0001t0076g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.736+4276C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889852 | |||||||
chr6:70889961 | T | C | 1 | a0001c0001t0004g0141 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.736+4167A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889961 | |||||||
chr6:70889970 | C | T | 1 | a0001c0001t0059g0163 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.736+4158G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889970 | |||||||
chr6:70889993 | G | A | 1 | a0001c0002t0005g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.736+4135C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70889993 | |||||||
chr6:70890028 | T | G | 3 | a0001c0001t0069g0104 a0001c0002t0042g0253 a0001c0002t0042g0294 |
3 | HG02717.hp1 HG03098.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.736+4100A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70890028 | |||||||
chr6:70890077 | C | T | 3 | a0001c0001t0010g0124 a0001c0001t0019g0024 a0001c0001t0019g0025 |
3 | HG00408.hp2 NA18945.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.736+4051G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70890077 | |||||||
chr6:70890085 | A | G | 8 | a0001c0001t0023g0077 a0001c0001t0023g0078 a0001c0001t0023g0087 others(5): Show |
8 | HG02559.hp1 HG02723.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.736+4043T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70890085 | |||||||
chr6:70890109 | T | G | 1 | a0001c0001t0073g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.736+4019A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70890109 | |||||||
chr6:70890123 | T | C | 17 | a0001c0001t0020g0054 a0001c0001t0020g0067 a0001c0001t0020g0079 others(14): Show |
17 | HG00323.hp1 HG01074.hp2 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.736+4005A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70890123 | |||||||
chr6:70890184 | A | G | 69 | a0001c0001t0001g0144 a0001c0001t0002g0001 a0001c0001t0002g0035 others(66): Show |
70 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.736+3944T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70890184 | |||||||
chr6:70890304 | T | C | 1 | a0002c0004t0063g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.736+3824A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70890304 | |||||||
chr6:70890588 | T | C | 1 | a0002c0004t0063g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.736+3540A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70890588 | |||||||
chr6:70890632 | T | C | 231 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(228): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.736+3496A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70890632 | |||||||
chr6:70890916 | T | C | 2 | a0001c0001t0003g0139 a0001c0002t0006g0197 |
2 | HG02895.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.736+3212A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70890916 | |||||||
chr6:70891019 | C | A | 1 | a0001c0001t0001g0065 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.736+3109G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891019 | |||||||
chr6:70891164 | T | C | 36 | a0001c0001t0001g0061 a0001c0001t0002g0066 a0001c0001t0002g0070 others(33): Show |
36 | HG00673.hp2 HG00741.hp1 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.736+2964A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891164 | |||||||
chr6:70891220 | A | G | 252 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(249): Show |
255 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.736+2908T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891220 | |||||||
chr6:70891385 | G | T | 1 | a0001c0001t0037g0062 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.736+2743C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891385 | |||||||
chr6:70891529 | T | G | 12 | a0001c0001t0010g0052 a0001c0001t0010g0072 a0001c0001t0010g0085 others(9): Show |
12 | HG01074.hp1 HG01099.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.736+2599A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891529 | |||||||
chr6:70891588 | C | G | 1 | a0001c0002t0040g0222 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.736+2540G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891588 | |||||||
chr6:70891620 | A | T | 1 | a0001c0001t0009g0096 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.736+2508T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891620 | |||||||
chr6:70891654 | G | A | 1 | a0001c0002t0011g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.736+2474C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891654 | |||||||
chr6:70891718 | T | C | 7 | a0001c0001t0013g0117 a0001c0002t0005g0214 a0001c0002t0005g0216 others(4): Show |
7 | NA18949.hp1 NA18960.hp2 NA18963.hp1 others(4): Show |
intron_variant | MODIFIER | c.736+2410A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891718 | |||||||
chr6:70891748 | T | TTG | 48 | a0001c0001t0001g0002 a0001c0001t0002g0060 a0001c0001t0002g0150 others(45): Show |
49 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.736+2378_736+2379d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891748 | |||||||
chr6:70891748 | T | TTGTG | 8 | a0001c0001t0003g0155 a0001c0001t0004g0053 a0001c0001t0004g0057 others(5): Show |
8 | HG00642.hp2 HG02258.hp2 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.736+2376_736+2379d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891748 | |||||||
chr6:70891748 | T | TTGTGTGT others(1): Show |
10 | a0001c0001t0001g0170 a0001c0001t0002g0066 a0001c0001t0002g0070 others(7): Show |
10 | HG00423.hp2 HG00673.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.736+2372_736+2379d others(10): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891748 | |||||||
chr6:70891748 | T | TTGTGTGT others(5): Show |
1 | a0001c0001t0010g0095 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.736+2368_736+2379d others(14): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891748 | |||||||
chr6:70891748 | TTG | T | 35 | a0001c0001t0001g0042 a0001c0001t0003g0100 a0001c0001t0003g0101 others(32): Show |
35 | HG01069.hp1 HG01074.hp2 HG01099.hp1 others(32): Show |
intron_variant | MODIFIER | c.736+2378_736+2379d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891748 | |||||||
chr6:70891748 | TTGTG | T | 6 | a0001c0002t0005g0202 a0001c0002t0021g0182 a0001c0002t0092g0264 others(3): Show |
6 | HG02647.hp2 HG02698.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.736+2376_736+2379d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891748 | |||||||
chr6:70891748 | TTGTGTG | T | 4 | a0001c0001t0013g0129 a0001c0002t0026g0242 a0001c0002t0042g0294 others(1): Show |
4 | HG03098.hp1 HG03927.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.736+2374_736+2379d others(8): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891748 | |||||||
chr6:70891748 | TTGTGTGT others(1): Show |
T | 12 | a0001c0001t0010g0052 a0001c0001t0010g0072 a0001c0001t0010g0085 others(9): Show |
12 | HG01074.hp1 HG01099.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.736+2372_736+2379d others(10): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891748 | |||||||
chr6:70891748 | TTGTGTGT others(7): Show |
T | 1 | a0001c0002t0081g0239 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.736+2366_736+2379d others(16): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891748 | |||||||
chr6:70891807 | T | C | 43 | a0001c0001t0001g0042 a0001c0001t0003g0100 a0001c0001t0003g0101 others(40): Show |
43 | HG00642.hp1 HG01069.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.736+2321A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70891807 | |||||||
chr6:70892195 | A | G | 1 | a0001c0002t0015g0284 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.736+1933T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892195 | |||||||
chr6:70892326 | G | A | 1 | a0001c0001t0003g0139 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.736+1802C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892326 | |||||||
chr6:70892338 | C | A | 1 | a0001c0001t0001g0002 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.736+1790G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892338 | |||||||
chr6:70892365 | C | G | 18 | a0001c0001t0001g0042 a0001c0001t0003g0100 a0001c0001t0003g0101 others(15): Show |
18 | HG00642.hp1 HG01074.hp2 HG01099.hp1 others(15): Show |
intron_variant | MODIFIER | c.736+1763G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892365 | |||||||
chr6:70892466 | G | A | 55 | a0001c0001t0001g0058 a0001c0001t0002g0001 a0001c0001t0002g0035 others(52): Show |
56 | HG00099.hp1 HG00741.hp1 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.736+1662C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892466 | |||||||
chr6:70892470 | T | G | 55 | a0001c0001t0001g0058 a0001c0001t0002g0001 a0001c0001t0002g0035 others(52): Show |
56 | HG00099.hp1 HG00741.hp1 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.736+1658A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892470 | |||||||
chr6:70892484 | T | C | 1 | a0001c0001t0004g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.736+1644A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892484 | |||||||
chr6:70892492 | C | A | 1 | a0001c0001t0103g0307 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.736+1636G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892492 | |||||||
chr6:70892717 | C | T | 113 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0047 others(110): Show |
115 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.736+1411G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892717 | |||||||
chr6:70892772 | C | T | 3 | a0001c0001t0003g0139 a0001c0001t0055g0131 a0001c0001t0069g0104 |
3 | HG02717.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.736+1356G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892772 | |||||||
chr6:70892816 | C | G | 3 | a0001c0001t0003g0139 a0001c0001t0055g0131 a0001c0001t0069g0104 |
3 | HG02717.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.736+1312G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892816 | |||||||
chr6:70892825 | C | T | 3 | a0001c0001t0004g0165 a0001c0001t0036g0105 a0001c0001t0036g0142 |
3 | HG02109.hp2 HG02809.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.736+1303G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892825 | |||||||
chr6:70892900 | A | C | 3 | a0001c0001t0003g0139 a0001c0001t0055g0131 a0001c0001t0069g0104 |
3 | HG02717.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.736+1228T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70892900 | |||||||
chr6:70893155 | T | C | 1 | a0001c0002t0021g0237 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.736+973A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70893155 | |||||||
chr6:70893268 | C | T | 1 | a0001c0001t0002g0122 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.736+860G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70893268 | |||||||
chr6:70893288 | A | G | 1 | a0001c0002t0042g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.736+840T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70893288 | |||||||
chr6:70893379 | T | A | 1 | a0001c0002t0042g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.736+749A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70893379 | |||||||
chr6:70893404 | A | AT | 117 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0047 others(114): Show |
119 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.736+723dupA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70893404 | |||||||
chr6:70893870 | C | T | 1 | a0001c0001t0057g0074 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.736+258G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70893870 | |||||||
chr6:70893898 | G | A | 1 | a0001c0002t0042g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.736+230C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70893898 | |||||||
chr6:70894081 | A | G | 2 | a0001c0002t0008g0247 a0001c0002t0098g0292 |
2 | HG02735.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.736+47T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 2/3 | chr6 | 70894081 | |||||||
chr6:70894406 | C | A | 1 | a0001c0002t0080g0194 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.592-134G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70894406 | |||||||
chr6:70894531 | A | G | 1 | a0001c0001t0069g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.592-259T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70894531 | |||||||
chr6:70894536 | T | A | 1 | a0001c0001t0069g0104 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.592-264A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70894536 | |||||||
chr6:70894707 | A | ACTTTTCT others(10): Show |
1 | a0001c0001t0001g0069 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.592-452_592-436dup others(17): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70894707 | |||||||
chr6:70894847 | A | T | 3 | a0001c0001t0001g0170 a0001c0001t0037g0062 a0001c0001t0074g0088 |
3 | HG03239.hp1 HG03669.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.592-575T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70894847 | |||||||
chr6:70894875 | C | T | 1 | a0001c0002t0091g0259 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.592-603G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70894875 | |||||||
chr6:70894924 | A | T | 1 | a0001c0001t0017g0008 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.592-652T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70894924 | |||||||
chr6:70895338 | T | A | 1 | a0001c0002t0005g0210 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.592-1066A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895338 | |||||||
chr6:70895495 | A | AT | 22 | a0001c0001t0002g0071 a0001c0001t0003g0137 a0001c0001t0010g0052 others(19): Show |
22 | HG01069.hp2 HG01167.hp2 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.592-1224dupA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895495 | |||||||
chr6:70895495 | A | ATT | 59 | a0001c0001t0001g0002 a0001c0001t0001g0049 a0001c0001t0001g0055 others(56): Show |
61 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.592-1225_592-1224d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895495 | |||||||
chr6:70895495 | A | ATTT | 46 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0056 others(43): Show |
46 | HG00408.hp2 HG00621.hp1 HG00621.hp2 others(43): Show |
intron_variant | MODIFIER | c.592-1226_592-1224d others(5): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895495 | |||||||
chr6:70895495 | A | T | 1 | a0001c0001t0017g0008 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.592-1223T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895495 | |||||||
chr6:70895495 | AT | A | 35 | a0001c0001t0002g0001 a0001c0001t0002g0066 a0001c0001t0002g0073 others(32): Show |
36 | HG00642.hp1 HG00673.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.592-1224delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895495 | |||||||
chr6:70895495 | ATT | A | 83 | a0001c0001t0001g0058 a0001c0001t0002g0035 a0001c0001t0002g0038 others(80): Show |
83 | HG00099.hp1 HG00423.hp2 HG00741.hp1 others(80): Show |
intron_variant | MODIFIER | c.592-1225_592-1224d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895495 | |||||||
chr6:70895528 | C | T | 1 | a0001c0001t0002g0038 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.592-1256G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895528 | |||||||
chr6:70895537 | A | ACTC | 115 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(112): Show |
117 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.592-1268_592-1266d others(5): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895537 | |||||||
chr6:70895688 | T | G | 1 | a0001c0002t0089g0297 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.592-1416A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895688 | |||||||
chr6:70895731 | G | A | 1 | a0001c0001t0004g0140 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.592-1459C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895731 | |||||||
chr6:70895833 | C | CT | 55 | a0001c0001t0001g0170 a0001c0001t0002g0066 a0001c0001t0002g0070 others(52): Show |
55 | HG00423.hp2 HG00642.hp1 HG00673.hp2 others(52): Show |
intron_variant | MODIFIER | c.592-1562dupA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895833 | |||||||
chr6:70895923 | GGTCTGCT others(12): Show |
G | 1 | a0001c0001t0001g0069 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.592-1670_592-1652d others(21): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895923 | |||||||
chr6:70895969 | T | C | 2 | a0001c0001t0003g0139 a0001c0001t0055g0131 |
2 | HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.592-1697A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895969 | |||||||
chr6:70895988 | C | T | 3 | a0001c0001t0003g0103 a0001c0001t0003g0127 a0001c0001t0004g0126 |
3 | HG00741.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.592-1716G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70895988 | |||||||
chr6:70896109 | G | A | 230 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(227): Show |
233 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(230): Show |
intron_variant | MODIFIER | c.592-1837C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896109 | |||||||
chr6:70896196 | CAGAG | C | 8 | a0001c0001t0023g0077 a0001c0001t0023g0078 a0001c0001t0025g0110 others(5): Show |
8 | HG01069.hp1 HG03139.hp2 HG03209.hp2 others(5): Show |
intron_variant | MODIFIER | c.592-1928_592-1925d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896196 | |||||||
chr6:70896324 | G | A | 1 | a0001c0001t0001g0055 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.592-2052C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896324 | |||||||
chr6:70896360 | C | T | 3 | a0001c0001t0003g0139 a0001c0001t0055g0131 a0001c0001t0069g0104 |
3 | HG02717.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.592-2088G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896360 | |||||||
chr6:70896452 | T | A | 1 | a0001c0002t0016g0236 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.592-2180A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896452 | |||||||
chr6:70896506 | A | C | 1 | a0001c0001t0003g0139 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.592-2234T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896506 | |||||||
chr6:70896532 | T | A | 3 | a0001c0001t0003g0103 a0001c0001t0003g0127 a0001c0001t0004g0126 |
3 | HG00741.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.592-2260A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896532 | |||||||
chr6:70896720 | CT | C | 9 | a0001c0001t0001g0170 a0001c0001t0037g0062 a0001c0001t0045g0004 others(6): Show |
9 | HG02559.hp1 HG02572.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.592-2449delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896720 | |||||||
chr6:70896731 | C | T | 1 | a0001c0002t0008g0218 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.592-2459G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896731 | |||||||
chr6:70896847 | C | T | 1 | a0001c0002t0030g0301 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.592-2575G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896847 | |||||||
chr6:70896910 | T | C | 18 | a0001c0001t0002g0066 a0001c0001t0002g0070 a0001c0001t0002g0073 others(15): Show |
18 | HG00423.hp2 HG00673.hp2 HG02015.hp1 others(15): Show |
intron_variant | MODIFIER | c.592-2638A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896910 | |||||||
chr6:70896978 | A | C | 1 | a0001c0001t0003g0132 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.592-2706T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70896978 | |||||||
chr6:70897023 | A | C | 1 | a0001c0001t0009g0096 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.592-2751T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897023 | |||||||
chr6:70897229 | A | C | 7 | a0001c0001t0019g0018 a0001c0001t0019g0030 a0001c0001t0036g0105 others(4): Show |
7 | HG01074.hp1 HG02027.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-2957T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897229 | |||||||
chr6:70897249 | CT | C | 108 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(105): Show |
110 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.592-2978delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897249 | |||||||
chr6:70897284 | C | T | 97 | a0001c0001t0001g0058 a0001c0001t0001g0170 a0001c0001t0002g0001 others(94): Show |
98 | HG00099.hp1 HG00423.hp2 HG00673.hp2 others(95): Show |
intron_variant | MODIFIER | c.592-3012G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897284 | |||||||
chr6:70897470 | C | T | 58 | a0001c0001t0001g0058 a0001c0001t0002g0001 a0001c0001t0002g0035 others(55): Show |
59 | HG00099.hp1 HG00741.hp1 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.592-3198G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897470 | |||||||
chr6:70897514 | G | A | 7 | a0001c0002t0005g0200 a0001c0002t0014g0286 a0001c0002t0014g0289 others(4): Show |
7 | HG00738.hp2 HG01167.hp2 HG01433.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-3242C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897514 | |||||||
chr6:70897522 | T | G | 7 | a0001c0001t0019g0018 a0001c0001t0019g0030 a0001c0001t0036g0105 others(4): Show |
7 | HG01074.hp1 HG02027.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-3250A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897522 | |||||||
chr6:70897607 | G | T | 1 | a0001c0001t0068g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.592-3335C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897607 | |||||||
chr6:70897658 | GAA | G | 7 | a0001c0001t0019g0018 a0001c0001t0019g0030 a0001c0001t0036g0105 others(4): Show |
7 | HG01074.hp1 HG02027.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-3388_592-3387d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897658 | |||||||
chr6:70897658 | GAAA | G | 6 | a0001c0001t0001g0170 a0001c0001t0003g0128 a0001c0001t0037g0062 others(3): Show |
6 | HG02451.hp2 HG02970.hp2 HG03239.hp1 others(3): Show |
intron_variant | MODIFIER | c.592-3389_592-3387d others(5): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897658 | |||||||
chr6:70897658 | GAAAA | G | 12 | a0001c0001t0003g0103 a0001c0001t0003g0127 a0001c0001t0003g0134 others(9): Show |
12 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(9): Show |
intron_variant | MODIFIER | c.592-3390_592-3387d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897658 | |||||||
chr6:70897667 | AAAAAT | A | 18 | a0001c0001t0003g0132 a0001c0001t0003g0139 a0001c0001t0004g0075 others(15): Show |
18 | HG01069.hp1 HG02559.hp1 HG02572.hp2 others(15): Show |
intron_variant | MODIFIER | c.592-3400_592-3396d others(7): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897667 | |||||||
chr6:70897668 | A | T | 4 | a0001c0001t0019g0018 a0001c0001t0019g0030 a0001c0002t0021g0237 others(1): Show |
4 | HG01074.hp1 HG02027.hp2 HG03927.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-3396T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897668 | |||||||
chr6:70897668 | AAAAT | A | 60 | a0001c0001t0001g0058 a0001c0001t0001g0144 a0001c0001t0002g0001 others(57): Show |
61 | HG00099.hp1 HG01884.hp1 HG02015.hp2 others(58): Show |
intron_variant | MODIFIER | c.592-3400_592-3397d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897668 | |||||||
chr6:70897669 | AAAT | A | 9 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0066g0143 others(6): Show |
9 | HG00621.hp1 HG02630.hp2 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.592-3400_592-3398d others(5): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897669 | |||||||
chr6:70897669 | AAATAT | A | 25 | a0001c0001t0003g0100 a0001c0001t0003g0101 a0001c0001t0020g0054 others(22): Show |
25 | HG00642.hp1 HG01074.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.592-3402_592-3398d others(7): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897669 | |||||||
chr6:70897670 | A | T | 10 | a0001c0001t0004g0053 a0001c0001t0004g0057 a0001c0001t0019g0018 others(7): Show |
10 | HG01074.hp1 HG02027.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.592-3398T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897670 | |||||||
chr6:70897670 | AATAT | A | 90 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0047 others(87): Show |
92 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.592-3402_592-3399d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897670 | |||||||
chr6:70897671 | ATAT | A | 11 | a0001c0001t0001g0044 a0001c0001t0001g0171 a0001c0001t0002g0066 others(8): Show |
11 | HG00423.hp2 HG00673.hp2 HG02698.hp1 others(8): Show |
intron_variant | MODIFIER | c.592-3402_592-3400d others(5): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897671 | |||||||
chr6:70897671 | ATATAT | A | 3 | a0001c0001t0019g0025 a0001c0001t0055g0131 a0001c0002t0042g0253 |
3 | HG03195.hp1 HG03453.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.592-3404_592-3400d others(7): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897671 | |||||||
chr6:70897672 | T | A | 3 | a0001c0002t0026g0180 a0001c0002t0026g0208 a0001c0002t0082g0238 |
3 | HG01099.hp2 HG02040.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.592-3400A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897672 | |||||||
chr6:70897676 | T | A | 14 | a0001c0001t0001g0044 a0001c0001t0001g0119 a0001c0001t0001g0161 others(11): Show |
14 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.592-3404A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897676 | |||||||
chr6:70897875 | G | C | 1 | a0001c0001t0068g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.592-3603C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897875 | |||||||
chr6:70897917 | T | C | 1 | a0001c0002t0042g0294 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.592-3645A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70897917 | |||||||
chr6:70898105 | T | C | 1 | a0002c0004t0063g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.592-3833A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70898105 | |||||||
chr6:70898111 | C | G | 1 | a0001c0002t0022g0281 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.592-3839G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70898111 | |||||||
chr6:70898146 | A | T | 14 | a0001c0001t0002g0066 a0001c0001t0002g0070 a0001c0001t0002g0073 others(11): Show |
14 | HG00423.hp2 HG00673.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.592-3874T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70898146 | |||||||
chr6:70898388 | T | TC | 9 | a0001c0001t0001g0042 a0001c0001t0002g0051 a0001c0001t0002g0159 others(6): Show |
9 | HG02145.hp1 HG02738.hp2 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.592-4117dupG | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70898388 | |||||||
chr6:70898472 | C | T | 1 | a0001c0001t0045g0004 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.592-4200G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70898472 | |||||||
chr6:70898515 | C | T | 7 | a0001c0001t0019g0018 a0001c0001t0019g0030 a0001c0001t0036g0105 others(4): Show |
7 | HG01074.hp1 HG02027.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-4243G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70898515 | |||||||
chr6:70898677 | A | T | 3 | a0001c0001t0003g0139 a0001c0001t0055g0131 a0001c0001t0069g0104 |
3 | HG02717.hp1 HG02895.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.592-4405T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70898677 | |||||||
chr6:70898963 | A | AAAAT | 24 | a0001c0001t0002g0151 a0001c0001t0003g0128 a0001c0001t0004g0165 others(21): Show |
24 | HG00408.hp1 HG00741.hp2 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.592-4695_592-4692d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70898963 | |||||||
chr6:70898963 | AAAAT | A | 40 | a0001c0001t0003g0139 a0001c0001t0004g0075 a0001c0001t0004g0140 others(37): Show |
40 | HG01069.hp1 HG01074.hp1 HG01433.hp1 others(37): Show |
intron_variant | MODIFIER | c.592-4695_592-4692d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70898963 | |||||||
chr6:70898987 | T | TAAATA | 5 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0066g0143 others(2): Show |
5 | HG02630.hp2 HG02647.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.592-4720_592-4716d others(7): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70898987 | |||||||
chr6:70899019 | A | G | 7 | a0001c0001t0004g0165 a0001c0002t0006g0186 a0001c0002t0006g0187 others(4): Show |
7 | HG02622.hp1 HG02630.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-4747T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899019 | |||||||
chr6:70899195 | T | C | 1 | a0001c0002t0080g0194 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.592-4923A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899195 | |||||||
chr6:70899239 | C | T | 1 | a0001c0001t0018g0013 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.592-4967G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899239 | |||||||
chr6:70899286 | T | C | 1 | a0001c0001t0049g0012 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.592-5014A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899286 | |||||||
chr6:70899302 | C | T | 4 | a0001c0001t0056g0116 a0001c0002t0006g0193 a0001c0002t0011g0255 others(1): Show |
4 | HG02559.hp2 HG02572.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-5030G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899302 | |||||||
chr6:70899346 | C | T | 28 | a0001c0001t0001g0064 a0001c0001t0002g0060 a0001c0001t0002g0150 others(25): Show |
28 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.592-5074G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899346 | |||||||
chr6:70899473 | G | C | 1 | a0001c0002t0014g0288 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.592-5201C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899473 | |||||||
chr6:70899488 | A | G | 5 | a0001c0002t0006g0229 a0001c0002t0006g0234 a0001c0002t0006g0245 others(2): Show |
5 | HG02165.hp1 HG02602.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-5216T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899488 | |||||||
chr6:70899520 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.592-5248G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899520 | |||||||
chr6:70899580 | T | TA | 7 | a0001c0001t0023g0077 a0001c0001t0023g0078 a0001c0001t0045g0004 others(4): Show |
7 | HG02559.hp1 HG03098.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-5309dupT | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899580 | |||||||
chr6:70899681 | A | G | 146 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0055 others(143): Show |
147 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.592-5409T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899681 | |||||||
chr6:70899728 | A | C | 1 | a0001c0001t0001g0065 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.592-5456T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899728 | |||||||
chr6:70899777 | G | A | 1 | a0001c0002t0022g0265 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.592-5505C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899777 | |||||||
chr6:70899784 | T | G | 5 | a0001c0001t0033g0115 a0001c0001t0056g0116 a0001c0002t0043g0273 others(2): Show |
5 | HG02970.hp2 HG02976.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.592-5512A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899784 | |||||||
chr6:70899788 | T | C | 1 | a0001c0001t0003g0139 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.592-5516A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899788 | |||||||
chr6:70899807 | G | C | 2 | a0001c0002t0006g0234 a0001c0002t0028g0221 |
2 | HG02165.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.592-5535C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899807 | |||||||
chr6:70899921 | A | G | 10 | a0001c0001t0001g0065 a0001c0001t0017g0008 a0001c0001t0017g0019 others(7): Show |
10 | HG01255.hp1 HG01981.hp2 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.592-5649T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899921 | |||||||
chr6:70899967 | G | A | 1 | a0001c0002t0042g0294 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.592-5695C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70899967 | |||||||
chr6:70900004 | A | C | 27 | a0001c0001t0002g0035 a0001c0001t0003g0169 a0001c0001t0013g0097 others(24): Show |
27 | HG00099.hp1 HG00597.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.592-5732T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70900004 | |||||||
chr6:70900124 | T | C | 7 | a0001c0001t0001g0002 a0001c0001t0001g0170 a0001c0001t0003g0155 others(4): Show |
8 | HG01074.hp1 HG01256.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.592-5852A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70900124 | |||||||
chr6:70900311 | G | C | 49 | a0001c0001t0001g0047 a0001c0001t0001g0049 a0001c0001t0004g0113 others(46): Show |
49 | HG00099.hp1 HG00642.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.592-6039C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70900311 | |||||||
chr6:70900409 | CT | C | 152 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0047 others(149): Show |
153 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.592-6138delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70900409 | |||||||
chr6:70900715 | C | T | 1 | a0001c0001t0068g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.592-6443G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70900715 | |||||||
chr6:70900753 | C | T | 4 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0048g0009 others(1): Show |
4 | HG02630.hp2 HG02723.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-6481G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70900753 | |||||||
chr6:70900793 | C | T | 2 | a0001c0001t0045g0004 a0001c0002t0042g0294 |
2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.592-6521G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70900793 | |||||||
chr6:70900926 | T | G | 1 | a0001c0001t0046g0017 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.592-6654A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70900926 | |||||||
chr6:70900958 | T | C | 1 | a0001c0002t0041g0189 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.592-6686A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70900958 | |||||||
chr6:70901075 | A | T | 40 | a0001c0001t0004g0075 a0001c0001t0053g0033 a0001c0001t0054g0032 others(37): Show |
40 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.592-6803T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70901075 | |||||||
chr6:70901093 | G | A | 60 | a0001c0001t0001g0002 a0001c0001t0001g0119 a0001c0001t0001g0144 others(57): Show |
61 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(58): Show |
intron_variant | MODIFIER | c.592-6821C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70901093 | |||||||
chr6:70901139 | T | C | 1 | a0001c0002t0006g0229 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.592-6867A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70901139 | |||||||
chr6:70901205 | C | T | 1 | a0001c0001t0109g0309 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.592-6933G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70901205 | |||||||
chr6:70901403 | G | A | 4 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0048g0009 others(1): Show |
4 | HG02630.hp2 HG02723.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-7131C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70901403 | |||||||
chr6:70901469 | C | T | 1 | a0001c0002t0007g0250 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.592-7197G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70901469 | |||||||
chr6:70901802 | C | T | 1 | a0001c0001t0013g0097 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.592-7530G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70901802 | |||||||
chr6:70901803 | G | A | 7 | a0001c0001t0004g0053 a0001c0001t0004g0057 a0001c0001t0023g0077 others(4): Show |
7 | HG02145.hp2 HG02258.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-7531C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70901803 | |||||||
chr6:70901844 | A | C | 1 | a0001c0002t0015g0287 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.592-7572T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70901844 | |||||||
chr6:70901893 | G | C | 1 | a0001c0001t0073g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.592-7621C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70901893 | |||||||
chr6:70902186 | C | T | 247 | a0001c0001t0001g0002 a0001c0001t0001g0044 a0001c0001t0001g0047 others(244): Show |
248 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.592-7914G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902186 | |||||||
chr6:70902334 | T | TA | 29 | a0001c0001t0001g0069 a0001c0001t0012g0026 a0001c0001t0012g0031 others(26): Show |
29 | HG00673.hp2 HG01074.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.592-8063dupT | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902334 | |||||||
chr6:70902363 | G | A | 12 | a0001c0002t0011g0269 a0001c0002t0022g0265 a0001c0002t0022g0268 others(9): Show |
12 | HG02132.hp1 HG02135.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.592-8091C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902363 | |||||||
chr6:70902412 | A | G | 1 | a0001c0001t0067g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.592-8140T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902412 | |||||||
chr6:70902617 | G | GAT | 39 | a0001c0001t0001g0069 a0001c0001t0003g0103 a0001c0001t0003g0127 others(36): Show |
39 | HG00735.hp1 HG00741.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.592-8347_592-8346d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | |||||||
chr6:70902617 | G | GATAT | 58 | a0001c0001t0001g0002 a0001c0001t0001g0119 a0001c0001t0001g0144 others(55): Show |
59 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.592-8349_592-8346d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | |||||||
chr6:70902617 | G | GATATAT | 7 | a0001c0001t0003g0128 a0001c0001t0019g0025 a0001c0001t0032g0005 others(4): Show |
7 | HG00323.hp1 HG01074.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.592-8351_592-8346d others(8): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | |||||||
chr6:70902617 | G | GATATATA others(1): Show |
14 | a0001c0001t0003g0169 a0001c0001t0012g0031 a0001c0001t0017g0008 others(11): Show |
14 | HG00673.hp2 HG01074.hp1 HG01168.hp1 others(11): Show |
intron_variant | MODIFIER | c.592-8353_592-8346d others(10): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | |||||||
chr6:70902617 | G | GATATATA others(3): Show |
2 | a0001c0001t0050g0022 a0001c0001t0066g0143 |
2 | NA18964.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.592-8355_592-8346d others(12): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | |||||||
chr6:70902617 | G | GATATATA others(7): Show |
1 | a0001c0001t0012g0026 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.592-8359_592-8346d others(16): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | |||||||
chr6:70902617 | G | GATATATA others(9): Show |
2 | a0001c0002t0011g0269 a0001c0002t0093g0267 |
2 | NA18965.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.592-8361_592-8346d others(18): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | |||||||
chr6:70902617 | G | GATATATA others(11): Show |
5 | a0001c0002t0030g0262 a0001c0002t0030g0263 a0001c0002t0030g0301 others(2): Show |
5 | HG02132.hp1 NA18951.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-8363_592-8346d others(20): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | |||||||
chr6:70902617 | G | GATATATA others(13): Show |
4 | a0001c0002t0022g0265 a0001c0002t0022g0268 a0001c0002t0029g0299 others(1): Show |
4 | HG02135.hp1 NA18981.hp2 NA19012.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-8365_592-8346d others(22): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | |||||||
chr6:70902617 | GAT | G | 69 | a0001c0001t0001g0102 a0001c0001t0001g0123 a0001c0001t0002g0001 others(66): Show |
71 | HG00423.hp2 HG00621.hp1 HG00621.hp2 others(68): Show |
intron_variant | MODIFIER | c.592-8347_592-8346d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | |||||||
chr6:70902617 | GATAT | G | 4 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0048g0009 others(1): Show |
4 | HG02630.hp2 HG02723.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.592-8349_592-8346d others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902617 | |||||||
chr6:70902627 | TATATATA others(9): Show |
T | 64 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0049 others(61): Show |
64 | HG00099.hp2 HG00408.hp2 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.592-8371_592-8356d others(18): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902627 | |||||||
chr6:70902631 | T | TACACACA others(1): Show |
3 | a0001c0001t0036g0105 a0001c0001t0036g0142 a0001c0001t0045g0004 |
3 | HG02109.hp2 HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.592-8360_592-8359i others(10): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902631 | |||||||
chr6:70902633 | T | C | 4 | a0001c0001t0036g0105 a0001c0001t0036g0142 a0001c0001t0045g0004 others(1): Show |
4 | HG02109.hp2 HG02559.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-8361A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902633 | |||||||
chr6:70902633 | T | TAC | 7 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(4): Show |
7 | HG02559.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.592-8362_592-8361i others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902633 | |||||||
chr6:70902633 | T | TACACACA others(5): Show |
1 | a0001c0001t0003g0082 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.592-8362_592-8361i others(14): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902633 | |||||||
chr6:70902635 | T | C | 14 | a0001c0001t0003g0082 a0001c0001t0036g0105 a0001c0001t0036g0142 others(11): Show |
14 | HG02109.hp2 HG02559.hp1 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.592-8363A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902635 | |||||||
chr6:70902637 | T | C | 30 | a0001c0001t0003g0082 a0001c0001t0003g0090 a0001c0001t0003g0091 others(27): Show |
30 | HG00597.hp2 HG01256.hp1 HG01496.hp1 others(27): Show |
intron_variant | MODIFIER | c.592-8365A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902637 | |||||||
chr6:70902637 | T | TATATATA others(17): Show |
1 | a0001c0002t0022g0298 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.592-8366_592-8365i others(26): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902637 | |||||||
chr6:70902637 | TAC | T | 8 | a0001c0001t0001g0042 a0001c0001t0003g0100 a0001c0001t0003g0101 others(5): Show |
8 | HG01884.hp2 HG02258.hp1 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.592-8367_592-8366d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902637 | |||||||
chr6:70902639 | C | T | 109 | a0001c0001t0001g0002 a0001c0001t0001g0069 a0001c0001t0001g0119 others(106): Show |
110 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(107): Show |
intron_variant | MODIFIER | c.592-8367G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902639 | |||||||
chr6:70902641 | C | T | 63 | a0001c0001t0001g0002 a0001c0001t0001g0069 a0001c0001t0001g0157 others(60): Show |
64 | HG00408.hp1 HG00544.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.592-8369G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902641 | |||||||
chr6:70902643 | C | T | 12 | a0001c0001t0003g0103 a0001c0001t0003g0127 a0001c0001t0004g0126 others(9): Show |
12 | HG00741.hp1 HG00741.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.592-8371G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902643 | |||||||
chr6:70902667 | T | C | 80 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0049 others(77): Show |
80 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.592-8395A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902667 | |||||||
chr6:70902669 | T | C | 1 | a0001c0002t0006g0197 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.592-8397A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902669 | |||||||
chr6:70902687 | C | G | 1 | a0001c0002t0042g0294 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.592-8415G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902687 | |||||||
chr6:70902767 | T | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0119 others(128): Show |
132 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.592-8495A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902767 | |||||||
chr6:70902788 | C | T | 1 | a0001c0001t0002g0153 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.592-8516G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70902788 | |||||||
chr6:70903193 | A | G | 8 | a0001c0001t0003g0100 a0001c0001t0003g0101 a0001c0001t0003g0136 others(5): Show |
8 | HG00323.hp2 HG01884.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.592-8921T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70903193 | |||||||
chr6:70903535 | T | C | 11 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0048g0009 others(8): Show |
11 | HG02630.hp2 HG02647.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.592-9263A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70903535 | |||||||
chr6:70903552 | T | C | 4 | a0001c0001t0003g0136 a0001c0001t0003g0137 a0001c0001t0025g0138 others(1): Show |
4 | HG01884.hp2 HG03225.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-9280A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70903552 | |||||||
chr6:70903746 | G | C | 2 | a0001c0001t0003g0082 a0001c0002t0042g0253 |
2 | HG03453.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.592-9474C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70903746 | |||||||
chr6:70903749 | C | T | 102 | a0001c0001t0001g0002 a0001c0001t0001g0119 a0001c0001t0001g0144 others(99): Show |
103 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.592-9477G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70903749 | |||||||
chr6:70903811 | C | T | 1 | a0001c0002t0029g0299 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.592-9539G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70903811 | |||||||
chr6:70903913 | T | C | 20 | a0001c0001t0003g0082 a0001c0001t0003g0132 a0001c0001t0003g0136 others(17): Show |
20 | HG01884.hp2 HG02132.hp1 HG02135.hp1 others(17): Show |
intron_variant | MODIFIER | c.592-9641A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70903913 | |||||||
chr6:70903948 | T | C | 253 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(250): Show |
254 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.592-9676A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70903948 | |||||||
chr6:70904044 | C | T | 185 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(182): Show |
186 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.592-9772G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70904044 | |||||||
chr6:70904152 | G | C | 183 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(180): Show |
184 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.592-9880C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70904152 | |||||||
chr6:70904198 | C | T | 1 | a0001c0002t0087g0235 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.592-9926G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70904198 | |||||||
chr6:70904406 | G | A | 75 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0049 others(72): Show |
75 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(72): Show |
intron_variant | MODIFIER | c.592-10134C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70904406 | |||||||
chr6:70904593 | C | T | 1 | a0001c0001t0033g0076 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.592-10321G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70904593 | |||||||
chr6:70904773 | A | C | 12 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0018g0007 others(9): Show |
12 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.592-10501T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70904773 | |||||||
chr6:70904808 | C | G | 1 | a0001c0001t0009g0096 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.592-10536G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70904808 | |||||||
chr6:70904959 | T | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(178): Show |
182 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.592-10687A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70904959 | |||||||
chr6:70904982 | C | A | 1 | a0001c0001t0003g0036 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.592-10710G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70904982 | |||||||
chr6:70905885 | CTG | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(213): Show |
217 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.592-11615_592-1161 others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70905885 | |||||||
chr6:70906149 | G | A | 2 | a0001c0002t0005g0232 a0001c0002t0005g0233 |
2 | NA18960.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.592-11877C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70906149 | |||||||
chr6:70906361 | G | C | 1 | a0001c0001t0004g0162 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.592-12089C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70906361 | |||||||
chr6:70906442 | C | A | 15 | a0001c0001t0001g0102 a0001c0001t0003g0090 a0001c0001t0003g0091 others(12): Show |
15 | HG00323.hp2 HG01256.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.592-12170G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70906442 | |||||||
chr6:70906565 | C | T | 3 | a0001c0002t0088g0296 a0001c0002t0089g0297 a0001c0002t0099g0290 |
3 | HG01074.hp2 HG02738.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.592-12293G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70906565 | |||||||
chr6:70906596 | A | T | 6 | a0001c0001t0018g0007 a0001c0001t0018g0013 a0001c0001t0018g0014 others(3): Show |
6 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.592-12324T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70906596 | |||||||
chr6:70906750 | A | C | 181 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(178): Show |
182 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.592-12478T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70906750 | |||||||
chr6:70907327 | G | A | 1 | a0001c0002t0021g0230 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.592-13055C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70907327 | |||||||
chr6:70907569 | T | C | 1 | a0001c0001t0001g0002 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.592-13297A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70907569 | |||||||
chr6:70907720 | G | C | 5 | a0001c0001t0002g0070 a0001c0001t0010g0052 a0001c0001t0010g0072 others(2): Show |
5 | HG01261.hp1 HG01891.hp2 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-13448C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70907720 | |||||||
chr6:70908127 | A | T | 6 | a0001c0001t0018g0007 a0001c0001t0018g0013 a0001c0001t0018g0014 others(3): Show |
6 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.592-13855T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70908127 | |||||||
chr6:70908296 | C | T | 12 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0018g0007 others(9): Show |
12 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.592-14024G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70908296 | |||||||
chr6:70908331 | G | C | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-14059C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70908331 | |||||||
chr6:70908465 | G | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(195): Show |
199 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.592-14193C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70908465 | |||||||
chr6:70908704 | G | A | 12 | a0001c0002t0011g0269 a0001c0002t0022g0265 a0001c0002t0022g0268 others(9): Show |
12 | HG02132.hp1 HG02135.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.592-14432C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70908704 | |||||||
chr6:70908929 | T | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(196): Show |
200 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.592-14657A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70908929 | |||||||
chr6:70909023 | A | C | 1 | a0001c0001t0001g0080 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.592-14751T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70909023 | |||||||
chr6:70909027 | T | C | 198 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(195): Show |
199 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.592-14755A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70909027 | |||||||
chr6:70909147 | C | T | 1 | a0001c0001t0109g0309 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.592-14875G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70909147 | |||||||
chr6:70909152 | T | A | 53 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(50): Show |
53 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.592-14880A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70909152 | |||||||
chr6:70909154 | A | T | 198 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(195): Show |
199 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.592-14882T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70909154 | |||||||
chr6:70909380 | G | A | 1 | a0001c0001t0073g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.592-15108C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70909380 | |||||||
chr6:70909383 | T | C | 3 | a0001c0002t0088g0296 a0001c0002t0089g0297 a0001c0002t0099g0290 |
3 | HG01074.hp2 HG02738.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.592-15111A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70909383 | |||||||
chr6:70909575 | G | A | 1 | a0001c0001t0003g0132 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.592-15303C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70909575 | |||||||
chr6:70909576 | C | T | 1 | a0001c0002t0082g0238 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.592-15304G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70909576 | |||||||
chr6:70909893 | A | G | 1 | a0001c0001t0012g0026 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.592-15621T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70909893 | |||||||
chr6:70910026 | A | G | 1 | a0001c0001t0073g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.592-15754T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70910026 | |||||||
chr6:70910040 | ATTTTTTG others(3): Show |
A | 39 | a0001c0002t0008g0249 a0001c0002t0011g0254 a0001c0002t0011g0255 others(36): Show |
39 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.592-15778_592-1576 others(14): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70910040 | |||||||
chr6:70910080 | G | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(194): Show |
198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.592-15808C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70910080 | |||||||
chr6:70910207 | G | A | 3 | a0001c0001t0003g0103 a0001c0001t0003g0127 a0001c0001t0004g0126 |
3 | HG00741.hp1 HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.592-15935C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70910207 | |||||||
chr6:70910364 | C | G | 1 | a0001c0001t0013g0117 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.592-16092G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70910364 | |||||||
chr6:70910378 | T | C | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-16106A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70910378 | |||||||
chr6:70910420 | C | T | 1 | a0001c0001t0020g0079 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.592-16148G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70910420 | |||||||
chr6:70910525 | G | A | 6 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0048g0009 others(3): Show |
6 | HG02630.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.592-16253C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70910525 | |||||||
chr6:70910682 | C | T | 2 | a0001c0001t0004g0113 a0001c0001t0025g0111 |
2 | HG02965.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.592-16410G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70910682 | |||||||
chr6:70910920 | T | C | 5 | a0001c0002t0005g0214 a0001c0002t0005g0231 a0001c0002t0005g0232 others(2): Show |
5 | NA18949.hp1 NA18960.hp2 NA19057.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-16648A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70910920 | |||||||
chr6:70911011 | T | A | 6 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0048g0009 others(3): Show |
6 | HG02630.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.592-16739A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70911011 | |||||||
chr6:70911375 | C | T | 1 | a0001c0002t0005g0216 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.592-17103G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70911375 | |||||||
chr6:70911888 | T | C | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-17616A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70911888 | |||||||
chr6:70911930 | T | C | 16 | a0001c0001t0001g0042 a0001c0001t0001g0102 a0001c0001t0003g0090 others(13): Show |
16 | HG00323.hp2 HG01256.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.592-17658A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70911930 | |||||||
chr6:70912411 | T | C | 1 | a0001c0001t0046g0017 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.592-18139A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912411 | |||||||
chr6:70912448 | T | C | 1 | a0001c0001t0010g0095 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.592-18176A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912448 | |||||||
chr6:70912497 | T | C | 1 | a0001c0001t0071g0039 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.592-18225A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912497 | |||||||
chr6:70912541 | T | C | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-18269A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912541 | |||||||
chr6:70912607 | C | T | 1 | a0001c0002t0011g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.592-18335G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912607 | |||||||
chr6:70912630 | AGCTGGCC others(15): Show |
A | 192 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(189): Show |
193 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.592-18380_592-1835 others(26): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912630 | |||||||
chr6:70912660 | TTATATCA others(14): Show |
T | 1 | a0001c0001t0019g0030 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.592-18409_592-1838 others(25): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912660 | |||||||
chr6:70912683 | T | C | 1 | a0001c0001t0047g0016 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.592-18411A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912683 | |||||||
chr6:70912763 | T | C | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-18491A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912763 | |||||||
chr6:70912783 | T | C | 250 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(247): Show |
251 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(248): Show |
intron_variant | MODIFIER | c.592-18511A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912783 | |||||||
chr6:70912829 | C | T | 1 | a0001c0001t0056g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.592-18557G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912829 | |||||||
chr6:70912934 | T | G | 1 | a0001c0002t0078g0206 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.592-18662A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70912934 | |||||||
chr6:70913032 | T | A | 1 | a0001c0001t0068g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.592-18760A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70913032 | |||||||
chr6:70913268 | G | T | 1 | a0001c0003t0062g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.592-18996C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70913268 | |||||||
chr6:70913290 | G | GGGTGTTT others(3): Show |
1 | a0001c0001t0052g0021 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.592-19028_592-1901 others(14): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70913290 | |||||||
chr6:70913550 | G | A | 168 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(165): Show |
169 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.592-19278C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70913550 | |||||||
chr6:70913594 | T | A | 1 | a0001c0002t0014g0288 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.592-19322A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70913594 | |||||||
chr6:70913834 | T | C | 2 | a0001c0001t0001g0144 a0001c0001t0034g0148 |
2 | NA18951.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.592-19562A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70913834 | |||||||
chr6:70913952 | G | C | 236 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(233): Show |
237 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.592-19680C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70913952 | |||||||
chr6:70914007 | A | G | 39 | a0001c0002t0008g0249 a0001c0002t0011g0254 a0001c0002t0011g0255 others(36): Show |
39 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.592-19735T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70914007 | |||||||
chr6:70914057 | C | T | 1 | a0001c0001t0001g0002 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.592-19785G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70914057 | |||||||
chr6:70914366 | A | T | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-20094T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70914366 | |||||||
chr6:70914753 | T | A | 1 | a0001c0002t0026g0180 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.592-20481A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70914753 | |||||||
chr6:70914760 | C | CT | 197 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(194): Show |
198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.592-20489dupA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70914760 | |||||||
chr6:70914810 | G | A | 4 | a0001c0001t0004g0113 a0001c0001t0025g0111 a0001c0001t0067g0114 others(1): Show |
4 | HG02886.hp2 HG02965.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-20538C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70914810 | |||||||
chr6:70914922 | C | T | 12 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0018g0007 others(9): Show |
12 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.592-20650G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70914922 | |||||||
chr6:70914938 | G | C | 16 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0172 others(13): Show |
16 | HG00408.hp2 HG00735.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.592-20666C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70914938 | |||||||
chr6:70915089 | A | G | 1 | a0001c0001t0002g0151 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.592-20817T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70915089 | |||||||
chr6:70915090 | T | C | 1 | a0001c0001t0050g0022 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.592-20818A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70915090 | |||||||
chr6:70915354 | T | C | 3 | a0001c0001t0009g0096 a0001c0001t0013g0097 a0001c0001t0037g0089 |
3 | HG01256.hp1 HG02055.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.592-21082A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70915354 | |||||||
chr6:70915360 | A | G | 1 | a0001c0001t0001g0063 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.592-21088T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70915360 | |||||||
chr6:70915582 | A | G | 1 | a0001c0002t0007g0213 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.592-21310T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70915582 | |||||||
chr6:70915896 | G | A | 13 | a0001c0001t0068g0168 a0001c0002t0011g0269 a0001c0002t0022g0265 others(10): Show |
13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.592-21624C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70915896 | |||||||
chr6:70916044 | C | A | 1 | a0001c0001t0002g0073 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.592-21772G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70916044 | |||||||
chr6:70916297 | G | A | 2 | a0001c0001t0019g0024 a0001c0001t0019g0025 |
2 | NA18945.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.592-22025C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70916297 | |||||||
chr6:70916312 | A | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(194): Show |
198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.592-22040T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70916312 | |||||||
chr6:70916441 | T | C | 1 | a0001c0001t0076g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.592-22169A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70916441 | |||||||
chr6:70916500 | G | C | 12 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0018g0007 others(9): Show |
12 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.592-22228C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70916500 | |||||||
chr6:70916508 | C | T | 1 | a0001c0001t0003g0128 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.592-22236G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70916508 | |||||||
chr6:70916586 | T | C | 1 | a0001c0003t0062g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.592-22314A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70916586 | |||||||
chr6:70916636 | T | A | 1 | a0001c0001t0004g0113 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.592-22364A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70916636 | |||||||
chr6:70917064 | C | T | 2 | a0001c0002t0005g0216 a0001c0002t0005g0217 |
2 | NA18963.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.592-22792G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70917064 | |||||||
chr6:70917234 | C | T | 12 | a0001c0002t0011g0269 a0001c0002t0022g0265 a0001c0002t0022g0268 others(9): Show |
12 | HG02132.hp1 HG02135.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.592-22962G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70917234 | |||||||
chr6:70917497 | G | A | 5 | a0001c0001t0003g0103 a0001c0001t0003g0127 a0001c0001t0004g0126 others(2): Show |
5 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.592-23225C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70917497 | |||||||
chr6:70917502 | T | C | 13 | a0001c0001t0068g0168 a0001c0002t0011g0269 a0001c0002t0022g0265 others(10): Show |
13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.592-23230A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70917502 | |||||||
chr6:70917765 | T | A | 1 | a0001c0001t0033g0115 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.592-23493A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70917765 | |||||||
chr6:70917905 | T | C | 39 | a0001c0002t0008g0249 a0001c0002t0011g0254 a0001c0002t0011g0255 others(36): Show |
39 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.592-23633A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70917905 | |||||||
chr6:70918113 | T | C | 1 | a0001c0002t0011g0271 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.592-23841A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70918113 | |||||||
chr6:70918337 | A | T | 39 | a0001c0002t0008g0249 a0001c0002t0011g0254 a0001c0002t0011g0255 others(36): Show |
39 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.592-24065T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70918337 | |||||||
chr6:70918679 | T | A | 1 | a0001c0001t0002g0174 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.592-24407A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70918679 | |||||||
chr6:70918763 | T | C | 1 | a0001c0002t0006g0234 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.592-24491A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70918763 | |||||||
chr6:70918825 | A | C | 5 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0080 others(2): Show |
5 | HG00099.hp2 HG02486.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.592-24553T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70918825 | |||||||
chr6:70919068 | G | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(194): Show |
198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.592-24796C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70919068 | |||||||
chr6:70919174 | C | T | 1 | a0001c0001t0002g0073 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.592-24902G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70919174 | |||||||
chr6:70919791 | G | A | 193 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(190): Show |
194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.592-25519C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70919791 | |||||||
chr6:70919900 | C | T | 2 | a0001c0001t0067g0114 a0001c0002t0005g0199 |
2 | HG01496.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.592-25628G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70919900 | |||||||
chr6:70919976 | C | T | 3 | a0001c0001t0002g0122 a0001c0001t0050g0022 a0001c0001t0052g0021 |
3 | NA18948.hp2 NA18964.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.592-25704G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70919976 | |||||||
chr6:70920038 | T | C | 1 | a0001c0002t0007g0213 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.592-25766A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70920038 | |||||||
chr6:70920056 | G | A | 180 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(177): Show |
181 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.592-25784C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70920056 | |||||||
chr6:70920089 | G | A | 198 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(195): Show |
199 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.592-25817C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70920089 | |||||||
chr6:70920091 | T | C | 39 | a0001c0002t0008g0249 a0001c0002t0011g0254 a0001c0002t0011g0255 others(36): Show |
39 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.592-25819A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70920091 | |||||||
chr6:70920248 | T | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(194): Show |
198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.592-25976A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70920248 | |||||||
chr6:70920272 | G | A | 2 | a0001c0001t0002g0121 a0001c0001t0103g0307 |
2 | HG01261.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.592-26000C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70920272 | |||||||
chr6:70920381 | G | A | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-26109C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70920381 | |||||||
chr6:70920574 | A | G | 1 | a0001c0002t0022g0298 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.592-26302T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70920574 | |||||||
chr6:70921291 | T | C | 25 | a0001c0002t0008g0249 a0001c0002t0014g0278 a0001c0002t0014g0283 others(22): Show |
25 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.592-27019A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70921291 | |||||||
chr6:70921425 | C | T | 1 | a0001c0001t0012g0031 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.592-27153G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70921425 | |||||||
chr6:70921531 | A | G | 168 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(165): Show |
169 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.592-27259T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70921531 | |||||||
chr6:70921819 | G | A | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-27547C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70921819 | |||||||
chr6:70921844 | A | G | 297 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(294): Show |
300 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(297): Show |
intron_variant | MODIFIER | c.592-27572T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70921844 | |||||||
chr6:70922120 | G | A | 39 | a0001c0002t0008g0249 a0001c0002t0011g0254 a0001c0002t0011g0255 others(36): Show |
39 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.592-27848C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70922120 | |||||||
chr6:70922195 | A | T | 2 | a0001c0002t0014g0291 a0001c0002t0029g0279 |
2 | HG00738.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.592-27923T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70922195 | |||||||
chr6:70922325 | T | C | 168 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(165): Show |
169 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.592-28053A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70922325 | |||||||
chr6:70922353 | T | C | 78 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0049 others(75): Show |
78 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.592-28081A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70922353 | |||||||
chr6:70922588 | A | T | 1 | a0001c0001t0010g0072 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.592-28316T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70922588 | |||||||
chr6:70922679 | G | T | 70 | a0001c0001t0001g0002 a0001c0001t0001g0119 a0001c0001t0001g0123 others(67): Show |
71 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.592-28407C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70922679 | |||||||
chr6:70922726 | T | C | 1 | a0001c0001t0056g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.592-28454A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70922726 | |||||||
chr6:70923300 | C | T | 2 | a0001c0001t0003g0090 a0001c0001t0003g0091 |
2 | NA18962.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.592-29028G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70923300 | |||||||
chr6:70923584 | A | G | 1 | a0001c0002t0031g0276 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.592-29312T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70923584 | |||||||
chr6:70923637 | C | T | 1 | a0001c0002t0006g0186 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.592-29365G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70923637 | |||||||
chr6:70923647 | G | C | 1 | a0001c0002t0043g0272 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.592-29375C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70923647 | |||||||
chr6:70923687 | C | A | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-29415G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70923687 | |||||||
chr6:70923786 | T | C | 1 | a0001c0001t0002g0174 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.592-29514A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70923786 | |||||||
chr6:70923818 | G | A | 1 | a0001c0001t0002g0121 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.592-29546C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70923818 | |||||||
chr6:70923836 | T | C | 1 | a0001c0002t0014g0289 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.592-29564A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70923836 | |||||||
chr6:70923904 | A | C | 1 | a0001c0001t0012g0031 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.592-29632T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70923904 | |||||||
chr6:70924658 | C | T | 1 | a0001c0002t0011g0254 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.592-30386G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70924658 | |||||||
chr6:70924859 | T | C | 1 | a0001c0001t0004g0099 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.592-30587A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70924859 | |||||||
chr6:70924905 | G | A | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.592-30633C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70924905 | |||||||
chr6:70924918 | T | C | 1 | a0001c0002t0042g0294 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.592-30646A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70924918 | |||||||
chr6:70925022 | G | A | 1 | a0001c0001t0061g0094 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.592-30750C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925022 | |||||||
chr6:70925023 | C | A | 1 | a0001c0001t0061g0094 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.592-30751G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925023 | |||||||
chr6:70925029 | A | T | 193 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(190): Show |
194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.592-30757T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925029 | |||||||
chr6:70925037 | G | A | 3 | a0001c0002t0016g0236 a0001c0002t0079g0201 a0001c0002t0087g0235 |
3 | HG00597.hp2 HG00621.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.592-30765C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925037 | |||||||
chr6:70925122 | C | G | 1 | a0001c0002t0021g0248 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.591+30717G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925122 | |||||||
chr6:70925123 | C | T | 60 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0049 others(57): Show |
60 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.591+30716G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925123 | |||||||
chr6:70925143 | C | A | 1 | a0001c0001t0013g0034 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.591+30696G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925143 | |||||||
chr6:70925180 | C | T | 1 | a0001c0001t0004g0165 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.591+30659G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925180 | |||||||
chr6:70925226 | G | A | 13 | a0001c0001t0068g0168 a0001c0002t0011g0269 a0001c0002t0022g0265 others(10): Show |
13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.591+30613C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925226 | |||||||
chr6:70925245 | C | G | 1 | a0001c0001t0067g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.591+30594G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925245 | |||||||
chr6:70925378 | G | C | 1 | a0001c0001t0013g0050 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.591+30461C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925378 | |||||||
chr6:70925407 | C | T | 1 | a0001c0003t0062g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.591+30432G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925407 | |||||||
chr6:70925408 | G | A | 2 | a0001c0001t0012g0026 a0001c0001t0046g0017 |
2 | HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.591+30431C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925408 | |||||||
chr6:70925455 | C | T | 1 | a0001c0003t0062g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.591+30384G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925455 | |||||||
chr6:70925513 | C | T | 1 | a0001c0001t0004g0099 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.591+30326G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925513 | |||||||
chr6:70925610 | C | T | 13 | a0001c0001t0068g0168 a0001c0002t0011g0269 a0001c0002t0022g0265 others(10): Show |
13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.591+30229G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70925610 | |||||||
chr6:70926026 | A | C | 1 | a0001c0002t0006g0190 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.591+29813T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926026 | |||||||
chr6:70926033 | G | A | 3 | a0001c0002t0038g0177 a0001c0002t0038g0179 a0001c0002t0077g0178 |
3 | NA18975.hp2 NA19056.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.591+29806C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926033 | |||||||
chr6:70926106 | A | T | 2 | a0001c0001t0003g0090 a0001c0001t0003g0091 |
2 | NA18962.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.591+29733T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926106 | |||||||
chr6:70926131 | C | G | 1 | a0001c0001t0003g0082 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.591+29708G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926131 | |||||||
chr6:70926210 | A | G | 4 | a0001c0002t0022g0265 a0001c0002t0030g0262 a0001c0002t0030g0263 others(1): Show |
4 | HG02135.hp1 NA18951.hp1 NA18962.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+29629T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926210 | |||||||
chr6:70926217 | G | A | 1 | a0002c0004t0063g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.591+29622C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926217 | |||||||
chr6:70926260 | C | T | 1 | a0001c0001t0009g0160 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.591+29579G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926260 | |||||||
chr6:70926261 | G | T | 13 | a0001c0001t0068g0168 a0001c0002t0011g0269 a0001c0002t0022g0265 others(10): Show |
13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.591+29578C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926261 | |||||||
chr6:70926279 | C | T | 1 | a0001c0001t0034g0107 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.591+29560G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926279 | |||||||
chr6:70926280 | G | A | 1 | a0001c0001t0002g0122 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.591+29559C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926280 | |||||||
chr6:70926377 | C | T | 193 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(190): Show |
194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.591+29462G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926377 | |||||||
chr6:70926397 | G | A | 3 | a0001c0001t0012g0031 a0001c0001t0032g0005 a0001c0001t0032g0027 |
3 | HG00673.hp2 NA18981.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.591+29442C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926397 | |||||||
chr6:70926578 | G | C | 1 | a0001c0002t0022g0268 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.591+29261C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926578 | |||||||
chr6:70926580 | T | C | 1 | a0001c0002t0043g0272 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.591+29259A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926580 | |||||||
chr6:70926590 | A | G | 4 | a0001c0001t0018g0013 a0001c0001t0018g0014 a0001c0001t0018g0015 others(1): Show |
4 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+29249T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926590 | |||||||
chr6:70926607 | G | T | 15 | a0001c0001t0001g0102 a0001c0001t0003g0090 a0001c0001t0003g0091 others(12): Show |
15 | HG00323.hp2 HG01256.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.591+29232C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926607 | |||||||
chr6:70926652 | G | A | 1 | a0001c0001t0001g0173 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.591+29187C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926652 | |||||||
chr6:70926682 | G | C | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+29157C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926682 | |||||||
chr6:70926684 | C | T | 1 | a0001c0002t0007g0211 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.591+29155G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926684 | |||||||
chr6:70926727 | A | G | 3 | a0001c0002t0014g0278 a0001c0002t0015g0252 a0001c0002t0097g0295 |
3 | HG00741.hp2 HG02300.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.591+29112T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926727 | |||||||
chr6:70926821 | C | G | 12 | a0001c0002t0011g0269 a0001c0002t0022g0265 a0001c0002t0022g0268 others(9): Show |
12 | HG02132.hp1 HG02135.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.591+29018G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926821 | |||||||
chr6:70926825 | A | T | 1 | a0001c0002t0015g0277 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.591+29014T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926825 | |||||||
chr6:70926909 | G | T | 2 | a0001c0001t0010g0085 a0001c0002t0031g0276 |
2 | HG01261.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.591+28930C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70926909 | |||||||
chr6:70927201 | A | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(194): Show |
198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.591+28638T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70927201 | |||||||
chr6:70927296 | A | T | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+28543T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70927296 | |||||||
chr6:70927385 | T | C | 4 | a0001c0002t0042g0253 a0001c0002t0042g0294 a0001c0002t0043g0272 others(1): Show |
4 | HG03098.hp1 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.591+28454A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70927385 | |||||||
chr6:70927454 | T | C | 2 | a0001c0001t0002g0051 a0001c0001t0002g0071 |
2 | NA18940.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.591+28385A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70927454 | |||||||
chr6:70927516 | G | A | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+28323C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70927516 | |||||||
chr6:70927765 | A | G | 1 | a0001c0003t0062g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.591+28074T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70927765 | |||||||
chr6:70927826 | C | A | 3 | a0001c0001t0004g0140 a0001c0001t0004g0141 a0001c0001t0036g0142 |
3 | HG02109.hp2 HG03130.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.591+28013G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70927826 | |||||||
chr6:70928019 | A | C | 1 | a0001c0001t0019g0018 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.591+27820T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928019 | |||||||
chr6:70928137 | G | A | 180 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(177): Show |
181 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.591+27702C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928137 | |||||||
chr6:70928177 | T | A | 2 | a0001c0002t0006g0245 a0001c0002t0016g0244 |
2 | HG03831.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.591+27662A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928177 | |||||||
chr6:70928177 | T | G | 1 | a0001c0001t0003g0128 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.591+27662A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928177 | |||||||
chr6:70928385 | C | A | 4 | a0001c0001t0010g0052 a0001c0001t0010g0072 a0001c0001t0010g0085 others(1): Show |
4 | HG01261.hp1 HG01891.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+27454G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928385 | |||||||
chr6:70928422 | A | G | 5 | a0001c0001t0003g0103 a0001c0001t0003g0127 a0001c0001t0004g0126 others(2): Show |
5 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.591+27417T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928422 | |||||||
chr6:70928592 | T | C | 16 | a0001c0001t0001g0042 a0001c0001t0001g0102 a0001c0001t0003g0090 others(13): Show |
16 | HG00323.hp2 HG01256.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.591+27247A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928592 | |||||||
chr6:70928702 | C | T | 1 | a0001c0002t0007g0250 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.591+27137G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928702 | |||||||
chr6:70928759 | C | A | 1 | a0001c0001t0013g0129 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.591+27080G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928759 | |||||||
chr6:70928796 | G | C | 74 | a0001c0001t0001g0002 a0001c0001t0001g0119 a0001c0001t0001g0123 others(71): Show |
75 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.591+27043C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928796 | |||||||
chr6:70928923 | A | C | 196 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(193): Show |
197 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.591+26916T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928923 | |||||||
chr6:70928923 | A | T | 1 | a0001c0001t0044g0305 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.591+26916T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70928923 | |||||||
chr6:70929236 | A | G | 12 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0018g0007 others(9): Show |
12 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.591+26603T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70929236 | |||||||
chr6:70929301 | A | AC | 197 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(194): Show |
198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.591+26537_591+2653 others(5): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70929301 | |||||||
chr6:70929421 | A | G | 1 | a0001c0002t0006g0190 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.591+26418T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70929421 | |||||||
chr6:70929437 | T | A | 60 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0049 others(57): Show |
60 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.591+26402A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70929437 | |||||||
chr6:70929455 | G | A | 1 | a0001c0001t0037g0089 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.591+26384C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70929455 | |||||||
chr6:70929523 | G | C | 78 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0049 others(75): Show |
78 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.591+26316C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70929523 | |||||||
chr6:70929548 | C | T | 6 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0048g0009 others(3): Show |
6 | HG02630.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.591+26291G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70929548 | |||||||
chr6:70929584 | C | T | 60 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0049 others(57): Show |
60 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.591+26255G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70929584 | |||||||
chr6:70929622 | G | A | 1 | a0001c0002t0016g0236 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.591+26217C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70929622 | |||||||
chr6:70929679 | T | C | 12 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0018g0007 others(9): Show |
12 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.591+26160A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70929679 | |||||||
chr6:70930088 | G | A | 39 | a0001c0002t0008g0249 a0001c0002t0011g0254 a0001c0002t0011g0255 others(36): Show |
39 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.591+25751C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70930088 | |||||||
chr6:70930286 | G | A | 78 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0049 others(75): Show |
78 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(75): Show |
intron_variant | MODIFIER | c.591+25553C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70930286 | |||||||
chr6:70930433 | A | C | 1 | a0001c0001t0001g0061 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.591+25406T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70930433 | |||||||
chr6:70930559 | C | T | 192 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(189): Show |
193 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.591+25280G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70930559 | |||||||
chr6:70930578 | C | T | 3 | a0001c0001t0017g0019 a0001c0001t0017g0020 a0001c0001t0017g0029 |
3 | HG01255.hp1 HG01981.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.591+25261G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70930578 | |||||||
chr6:70930615 | A | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(194): Show |
198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.591+25224T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70930615 | |||||||
chr6:70930955 | T | C | 1 | a0001c0001t0003g0090 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.591+24884A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70930955 | |||||||
chr6:70930984 | C | T | 1 | a0001c0002t0029g0275 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.591+24855G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70930984 | |||||||
chr6:70930994 | C | T | 2 | a0001c0001t0003g0100 a0001c0001t0003g0101 |
2 | HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.591+24845G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70930994 | |||||||
chr6:70931069 | C | G | 1 | a0001c0002t0005g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.591+24770G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70931069 | |||||||
chr6:70931075 | A | G | 1 | a0001c0002t0021g0237 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.591+24764T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70931075 | |||||||
chr6:70931189 | T | TG | 24 | a0001c0001t0001g0102 a0001c0001t0001g0123 a0001c0001t0002g0151 others(21): Show |
24 | HG00408.hp1 HG00408.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.591+24649dupC | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70931189 | |||||||
chr6:70931264 | G | A | 1 | a0001c0001t0034g0107 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.591+24575C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70931264 | |||||||
chr6:70931680 | G | T | 1 | a0001c0001t0001g0044 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.591+24159C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70931680 | |||||||
chr6:70931821 | G | A | 3 | a0001c0002t0088g0296 a0001c0002t0089g0297 a0001c0002t0099g0290 |
3 | HG01074.hp2 HG02738.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.591+24018C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70931821 | |||||||
chr6:70931821 | G | T | 13 | a0001c0001t0068g0168 a0001c0002t0011g0269 a0001c0002t0022g0265 others(10): Show |
13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.591+24018C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70931821 | |||||||
chr6:70932184 | C | T | 13 | a0001c0001t0068g0168 a0001c0002t0011g0269 a0001c0002t0022g0265 others(10): Show |
13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.591+23655G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70932184 | |||||||
chr6:70933129 | C | A | 1 | a0001c0002t0005g0240 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.591+22710G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70933129 | |||||||
chr6:70933570 | T | C | 1 | a0001c0002t0084g0243 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.591+22269A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70933570 | |||||||
chr6:70933687 | T | C | 203 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(200): Show |
205 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.591+22152A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70933687 | |||||||
chr6:70933701 | G | A | 39 | a0001c0002t0008g0249 a0001c0002t0011g0254 a0001c0002t0011g0255 others(36): Show |
39 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.591+22138C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70933701 | |||||||
chr6:70933731 | C | T | 1 | a0001c0002t0008g0215 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.591+22108G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70933731 | |||||||
chr6:70933858 | T | A | 7 | a0001c0001t0001g0144 a0001c0001t0003g0145 a0001c0001t0003g0146 others(4): Show |
7 | HG00423.hp1 HG00544.hp2 HG02129.hp1 others(4): Show |
intron_variant | MODIFIER | c.591+21981A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70933858 | |||||||
chr6:70934050 | G | A | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+21789C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70934050 | |||||||
chr6:70934366 | C | A | 1 | a0001c0001t0002g0059 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.591+21473G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70934366 | |||||||
chr6:70934461 | T | C | 1 | a0001c0001t0004g0075 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.591+21378A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70934461 | |||||||
chr6:70934480 | C | A | 15 | a0001c0001t0001g0102 a0001c0001t0003g0090 a0001c0001t0003g0091 others(12): Show |
15 | HG00323.hp2 HG01256.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.591+21359G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70934480 | |||||||
chr6:70934770 | A | C | 1 | a0001c0001t0003g0036 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.591+21069T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70934770 | |||||||
chr6:70934800 | G | A | 1 | a0001c0001t0004g0165 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.591+21039C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70934800 | |||||||
chr6:70935217 | G | A | 4 | a0001c0002t0042g0253 a0001c0002t0042g0294 a0001c0002t0043g0272 others(1): Show |
4 | HG03098.hp1 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.591+20622C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70935217 | |||||||
chr6:70935408 | C | T | 1 | a0001c0001t0009g0093 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.591+20431G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70935408 | |||||||
chr6:70935456 | T | G | 1 | a0001c0001t0073g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.591+20383A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70935456 | |||||||
chr6:70935530 | T | C | 1 | a0001c0002t0098g0292 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.591+20309A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70935530 | |||||||
chr6:70935700 | G | T | 5 | a0001c0001t0003g0100 a0001c0001t0003g0101 a0001c0001t0004g0099 others(2): Show |
5 | HG00323.hp2 HG01975.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.591+20139C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70935700 | |||||||
chr6:70935737 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.591+20102C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70935737 | |||||||
chr6:70935767 | A | G | 1 | a0001c0002t0084g0243 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.591+20072T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70935767 | |||||||
chr6:70935777 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.591+20062C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70935777 | |||||||
chr6:70935841 | C | T | 1 | a0001c0001t0056g0116 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.591+19998G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70935841 | |||||||
chr6:70936015 | G | A | 12 | a0001c0002t0011g0269 a0001c0002t0022g0265 a0001c0002t0022g0268 others(9): Show |
12 | HG02132.hp1 HG02135.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.591+19824C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936015 | |||||||
chr6:70936053 | G | A | 7 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(4): Show |
7 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.591+19786C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936053 | |||||||
chr6:70936069 | A | C | 1 | a0001c0002t0005g0214 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.591+19770T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936069 | |||||||
chr6:70936160 | C | T | 1 | a0001c0001t0002g0152 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.591+19679G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936160 | |||||||
chr6:70936282 | A | G | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+19557T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936282 | |||||||
chr6:70936326 | G | C | 5 | a0001c0001t0017g0029 a0001c0001t0036g0105 a0001c0001t0045g0004 others(2): Show |
5 | HG02004.hp2 HG02559.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.591+19513C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936326 | |||||||
chr6:70936352 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.591+19487T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936352 | |||||||
chr6:70936402 | C | T | 4 | a0001c0002t0006g0186 a0001c0002t0006g0187 a0001c0002t0006g0188 others(1): Show |
4 | HG02622.hp1 HG02630.hp1 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.591+19437G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936402 | |||||||
chr6:70936408 | A | G | 1 | a0001c0002t0007g0213 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.591+19431T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936408 | |||||||
chr6:70936432 | C | A | 2 | a0001c0001t0053g0033 a0001c0001t0054g0032 |
2 | HG02818.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.591+19407G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936432 | |||||||
chr6:70936444 | A | G | 1 | a0001c0001t0064g0166 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.591+19395T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936444 | |||||||
chr6:70936445 | A | T | 8 | a0001c0001t0064g0166 a0001c0002t0005g0202 a0001c0002t0006g0207 others(5): Show |
8 | HG00423.hp2 HG00621.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.591+19394T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936445 | |||||||
chr6:70936610 | C | T | 1 | a0001c0001t0037g0062 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.591+19229G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936610 | |||||||
chr6:70936737 | G | A | 2 | a0001c0001t0017g0008 a0001c0001t0019g0030 |
2 | NA19078.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.591+19102C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936737 | |||||||
chr6:70936741 | T | C | 3 | a0001c0001t0017g0008 a0001c0001t0019g0030 a0001c0002t0028g0251 |
3 | HG02738.hp2 NA19078.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.591+19098A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936741 | |||||||
chr6:70936806 | G | A | 15 | a0001c0001t0001g0102 a0001c0001t0003g0090 a0001c0001t0003g0091 others(12): Show |
15 | HG00323.hp2 HG01256.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.591+19033C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936806 | |||||||
chr6:70936809 | C | T | 1 | a0001c0002t0027g0212 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.591+19030G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70936809 | |||||||
chr6:70937012 | C | A | 1 | a0001c0001t0001g0102 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.591+18827G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937012 | |||||||
chr6:70937117 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.591+18722A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937117 | |||||||
chr6:70937251 | C | G | 193 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(190): Show |
194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.591+18588G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937251 | |||||||
chr6:70937299 | T | G | 13 | a0001c0001t0068g0168 a0001c0002t0011g0269 a0001c0002t0022g0265 others(10): Show |
13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.591+18540A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937299 | |||||||
chr6:70937306 | C | T | 17 | a0001c0001t0012g0023 a0001c0001t0012g0026 a0001c0001t0012g0028 others(14): Show |
17 | HG00673.hp2 HG01074.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.591+18533G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937306 | |||||||
chr6:70937327 | G | A | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+18512C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937327 | |||||||
chr6:70937571 | A | G | 1 | a0001c0001t0002g0060 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.591+18268T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937571 | |||||||
chr6:70937601 | T | C | 2 | a0001c0001t0001g0002 a0001c0001t0001g0170 |
3 | HG03490.hp2 HG03492.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.591+18238A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937601 | |||||||
chr6:70937704 | G | A | 1 | a0001c0002t0084g0243 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.591+18135C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937704 | |||||||
chr6:70937761 | T | C | 4 | a0001c0001t0004g0162 a0001c0001t0004g0164 a0001c0001t0004g0165 others(1): Show |
4 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+18078A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937761 | |||||||
chr6:70937905 | C | T | 28 | a0001c0001t0001g0002 a0001c0001t0001g0144 a0001c0001t0001g0157 others(25): Show |
29 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.591+17934G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937905 | |||||||
chr6:70937913 | C | T | 1 | a0001c0001t0003g0155 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.591+17926G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937913 | |||||||
chr6:70937951 | G | A | 15 | a0001c0001t0001g0102 a0001c0001t0003g0090 a0001c0001t0003g0091 others(12): Show |
15 | HG00323.hp2 HG01256.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.591+17888C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937951 | |||||||
chr6:70937953 | G | A | 168 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(165): Show |
169 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.591+17886C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937953 | |||||||
chr6:70937978 | C | T | 181 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(178): Show |
182 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.591+17861G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937978 | |||||||
chr6:70937997 | C | G | 2 | a0001c0001t0004g0075 a0001c0002t0005g0202 |
2 | NA19005.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.591+17842G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70937997 | |||||||
chr6:70938018 | A | C | 1 | a0001c0001t0003g0132 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.591+17821T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938018 | |||||||
chr6:70938145 | CA | C | 3 | a0001c0002t0030g0262 a0001c0002t0030g0263 a0001c0002t0092g0264 |
3 | NA18951.hp1 NA18962.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.591+17693delT | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938145 | |||||||
chr6:70938146 | AT | A | 9 | a0001c0002t0011g0269 a0001c0002t0022g0265 a0001c0002t0022g0268 others(6): Show |
9 | HG02132.hp1 HG02135.hp1 NA18965.hp1 others(6): Show |
intron_variant | MODIFIER | c.591+17692delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938146 | |||||||
chr6:70938147 | T | C | 3 | a0001c0002t0030g0262 a0001c0002t0030g0263 a0001c0002t0092g0264 |
3 | NA18951.hp1 NA18962.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.591+17692A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938147 | |||||||
chr6:70938193 | C | A | 1 | a0001c0003t0062g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.591+17646G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938193 | |||||||
chr6:70938242 | T | C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(190): Show |
194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.591+17597A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938242 | |||||||
chr6:70938243 | G | A | 193 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(190): Show |
194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.591+17596C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938243 | |||||||
chr6:70938255 | GATAC | G | 192 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(189): Show |
193 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.591+17580_591+1758 others(8): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938255 | |||||||
chr6:70938257 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.591+17582A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938257 | |||||||
chr6:70938261 | A | AATGGAAG others(20664): Show |
1 | a0001c0001t0001g0061 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.591+17577_591+1757 others(20675): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938261 | |||||||
chr6:70938261 | A | C | 192 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(189): Show |
193 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.591+17578T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938261 | |||||||
chr6:70938292 | T | C | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+17547A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938292 | |||||||
chr6:70938308 | T | C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(190): Show |
194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.591+17531A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938308 | |||||||
chr6:70938309 | G | C | 193 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(190): Show |
194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.591+17530C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938309 | |||||||
chr6:70938335 | A | G | 1 | a0001c0001t0066g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.591+17504T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938335 | |||||||
chr6:70938413 | T | C | 1 | a0001c0001t0013g0097 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.591+17426A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938413 | |||||||
chr6:70938425 | T | A | 1 | a0001c0001t0013g0097 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.591+17414A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938425 | |||||||
chr6:70938432 | G | A | 2 | a0001c0001t0003g0132 a0001c0001t0013g0097 |
2 | HG01256.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.591+17407C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938432 | |||||||
chr6:70938440 | C | T | 6 | a0001c0001t0003g0103 a0001c0001t0003g0127 a0001c0001t0004g0126 others(3): Show |
6 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.591+17399G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938440 | |||||||
chr6:70938676 | A | G | 5 | a0001c0001t0004g0053 a0001c0001t0044g0303 a0001c0001t0044g0305 others(2): Show |
5 | HG00735.hp1 HG01257.hp2 HG01261.hp2 others(2): Show |
intron_variant | MODIFIER | c.591+17163T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938676 | |||||||
chr6:70938677 | G | A | 4 | a0001c0001t0044g0303 a0001c0001t0044g0305 a0001c0001t0103g0307 others(1): Show |
4 | HG00735.hp1 HG01257.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+17162C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938677 | |||||||
chr6:70938981 | A | T | 1 | a0001c0002t0106g0308 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.591+16858T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938981 | |||||||
chr6:70938984 | A | T | 1 | a0001c0002t0106g0308 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.591+16855T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70938984 | |||||||
chr6:70939074 | C | G | 4 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0048g0009 others(1): Show |
4 | HG02630.hp2 HG02723.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.591+16765G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939074 | |||||||
chr6:70939086 | G | A | 1 | a0001c0001t0002g0073 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.591+16753C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939086 | |||||||
chr6:70939109 | C | A | 1 | a0001c0001t0067g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.591+16730G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939109 | |||||||
chr6:70939285 | T | A | 8 | a0001c0002t0011g0254 a0001c0002t0011g0255 a0001c0002t0011g0258 others(5): Show |
8 | HG02647.hp2 HG02717.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.591+16554A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939285 | |||||||
chr6:70939336 | C | T | 6 | a0001c0001t0033g0115 a0001c0001t0036g0105 a0001c0001t0044g0303 others(3): Show |
6 | HG00735.hp1 HG02071.hp2 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.591+16503G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939336 | |||||||
chr6:70939369 | C | T | 29 | a0001c0001t0001g0002 a0001c0001t0001g0144 a0001c0001t0001g0157 others(26): Show |
30 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.591+16470G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939369 | |||||||
chr6:70939426 | T | C | 1 | a0001c0001t0058g0083 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.591+16413A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939426 | |||||||
chr6:70939441 | T | C | 1 | a0001c0001t0019g0018 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.591+16398A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939441 | |||||||
chr6:70939461 | A | G | 37 | a0001c0001t0001g0002 a0001c0001t0001g0144 a0001c0001t0001g0157 others(34): Show |
38 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.591+16378T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939461 | |||||||
chr6:70939597 | G | A | 193 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(190): Show |
194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.591+16242C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939597 | |||||||
chr6:70939612 | T | C | 1 | a0001c0002t0014g0291 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.591+16227A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939612 | |||||||
chr6:70939619 | T | G | 8 | a0001c0002t0011g0254 a0001c0002t0011g0255 a0001c0002t0011g0258 others(5): Show |
8 | HG02647.hp2 HG02717.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.591+16220A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939619 | |||||||
chr6:70939662 | C | T | 13 | a0001c0001t0068g0168 a0001c0002t0011g0269 a0001c0002t0022g0265 others(10): Show |
13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.591+16177G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939662 | |||||||
chr6:70939663 | G | A | 2 | a0001c0002t0006g0245 a0001c0002t0016g0244 |
2 | HG03831.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.591+16176C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939663 | |||||||
chr6:70939705 | A | G | 196 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(193): Show |
197 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.591+16134T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939705 | |||||||
chr6:70939721 | A | G | 1 | a0001c0001t0002g0059 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.591+16118T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939721 | |||||||
chr6:70939755 | T | G | 12 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0018g0007 others(9): Show |
12 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.591+16084A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939755 | |||||||
chr6:70939756 | T | A | 12 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0018g0007 others(9): Show |
12 | HG01256.hp2 HG01257.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.591+16083A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939756 | |||||||
chr6:70939801 | T | G | 1 | a0001c0002t0039g0246 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.591+16038A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939801 | |||||||
chr6:70939936 | A | T | 9 | a0001c0002t0005g0202 a0001c0002t0005g0210 a0001c0002t0006g0207 others(6): Show |
9 | HG00423.hp2 HG00621.hp2 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.591+15903T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70939936 | |||||||
chr6:70940000 | G | A | 1 | a0001c0001t0003g0139 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.591+15839C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70940000 | |||||||
chr6:70940157 | C | T | 1 | a0001c0001t0003g0082 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.591+15682G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70940157 | |||||||
chr6:70940384 | G | A | 5 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0080 others(2): Show |
5 | HG00099.hp2 HG02486.hp1 HG02683.hp2 others(2): Show |
intron_variant | MODIFIER | c.591+15455C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70940384 | |||||||
chr6:70940469 | A | C | 197 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(194): Show |
198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.591+15370T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70940469 | |||||||
chr6:70940509 | C | G | 4 | a0001c0001t0001g0171 a0001c0001t0003g0169 a0001c0001t0035g0167 others(1): Show |
4 | HG01168.hp1 HG01169.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.591+15330G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70940509 | |||||||
chr6:70940601 | C | T | 1 | a0001c0001t0046g0017 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.591+15238G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70940601 | |||||||
chr6:70940653 | C | G | 1 | a0001c0002t0079g0201 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.591+15186G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70940653 | |||||||
chr6:70940699 | G | A | 39 | a0001c0002t0008g0249 a0001c0002t0011g0254 a0001c0002t0011g0255 others(36): Show |
39 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.591+15140C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70940699 | |||||||
chr6:70940814 | G | T | 2 | a0001c0002t0008g0249 a0001c0002t0094g0274 |
2 | HG00099.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.591+15025C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70940814 | |||||||
chr6:70940843 | G | A | 9 | a0001c0001t0003g0103 a0001c0001t0003g0127 a0001c0001t0004g0126 others(6): Show |
9 | HG00741.hp1 HG01167.hp1 HG01169.hp1 others(6): Show |
intron_variant | MODIFIER | c.591+14996C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70940843 | |||||||
chr6:70941091 | G | T | 2 | a0001c0001t0018g0007 a0001c0001t0051g0006 |
2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.591+14748C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70941091 | |||||||
chr6:70941333 | T | G | 4 | a0001c0001t0003g0132 a0001c0001t0003g0136 a0001c0001t0003g0137 others(1): Show |
4 | HG01884.hp2 HG02572.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+14506A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70941333 | |||||||
chr6:70941336 | T | A | 193 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(190): Show |
194 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.591+14503A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70941336 | |||||||
chr6:70941562 | A | T | 1 | a0001c0002t0011g0270 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.591+14277T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70941562 | |||||||
chr6:70941602 | TA | T | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+14236delT | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70941602 | |||||||
chr6:70941682 | C | G | 197 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(194): Show |
198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.591+14157G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70941682 | |||||||
chr6:70941811 | T | C | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+14028A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70941811 | |||||||
chr6:70941940 | T | C | 17 | a0001c0001t0012g0023 a0001c0001t0012g0026 a0001c0001t0012g0028 others(14): Show |
17 | HG00673.hp2 HG01074.hp1 HG01255.hp1 others(14): Show |
intron_variant | MODIFIER | c.591+13899A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70941940 | |||||||
chr6:70942642 | G | T | 197 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(194): Show |
198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.591+13197C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70942642 | |||||||
chr6:70942845 | G | A | 197 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(194): Show |
198 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(195): Show |
intron_variant | MODIFIER | c.591+12994C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70942845 | |||||||
chr6:70942924 | T | G | 1 | a0001c0001t0037g0089 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.591+12915A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70942924 | |||||||
chr6:70943044 | C | T | 2 | a0001c0001t0001g0002 a0001c0001t0001g0170 |
3 | HG03490.hp2 HG03492.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.591+12795G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70943044 | |||||||
chr6:70943246 | G | A | 1 | a0001c0002t0038g0179 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.591+12593C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70943246 | |||||||
chr6:70943346 | A | G | 1 | a0001c0001t0003g0128 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.591+12493T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70943346 | |||||||
chr6:70943580 | T | C | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+12259A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70943580 | |||||||
chr6:70943805 | G | A | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+12034C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70943805 | |||||||
chr6:70943858 | G | T | 15 | a0001c0001t0001g0102 a0001c0001t0003g0090 a0001c0001t0003g0091 others(12): Show |
15 | HG00323.hp2 HG01256.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.591+11981C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70943858 | |||||||
chr6:70943975 | T | C | 1 | a0001c0001t0068g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.591+11864A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70943975 | |||||||
chr6:70944004 | A | G | 1 | a0001c0002t0005g0200 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.591+11835T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944004 | |||||||
chr6:70944122 | G | T | 69 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0144 others(66): Show |
69 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.591+11717C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944122 | |||||||
chr6:70944194 | A | G | 233 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.591+11645T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944194 | |||||||
chr6:70944215 | C | G | 1 | a0002c0004t0063g0175 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.591+11624G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944215 | |||||||
chr6:70944346 | C | T | 1 | a0001c0001t0068g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.591+11493G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944346 | |||||||
chr6:70944357 | G | A | 57 | a0001c0002t0005g0181 a0001c0002t0005g0200 a0001c0002t0005g0202 others(54): Show |
58 | HG00423.hp2 HG00597.hp2 HG00621.hp1 others(55): Show |
intron_variant | MODIFIER | c.591+11482C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944357 | |||||||
chr6:70944390 | A | G | 1 | a0001c0001t0001g0056 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.591+11449T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944390 | |||||||
chr6:70944435 | G | GCTCGGAG others(7): Show |
224 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.591+11403_591+1140 others(18): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944435 | |||||||
chr6:70944435 | G | GCTTGGAG others(7): Show |
13 | a0001c0001t0068g0168 a0001c0002t0011g0269 a0001c0002t0022g0265 others(10): Show |
13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.591+11403_591+1140 others(18): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944435 | |||||||
chr6:70944501 | G | A | 1 | a0001c0001t0066g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.591+11338C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944501 | |||||||
chr6:70944501 | G | T | 4 | a0001c0001t0004g0162 a0001c0001t0004g0164 a0001c0001t0004g0165 others(1): Show |
4 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+11338C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944501 | |||||||
chr6:70944615 | C | T | 29 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0012g0023 others(26): Show |
29 | HG00673.hp2 HG01074.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.591+11224G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944615 | |||||||
chr6:70944630 | CCT | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.591+11207_591+1120 others(6): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944630 | |||||||
chr6:70944836 | C | A | 1 | a0001c0001t0003g0128 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.591+11003G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944836 | |||||||
chr6:70944849 | C | T | 6 | a0001c0001t0001g0102 a0001c0001t0003g0090 a0001c0001t0003g0091 others(3): Show |
6 | HG02015.hp1 NA18940.hp1 NA18962.hp1 others(3): Show |
intron_variant | MODIFIER | c.591+10990G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944849 | |||||||
chr6:70944865 | T | C | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+10974A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944865 | |||||||
chr6:70944901 | C | G | 15 | a0001c0001t0001g0102 a0001c0001t0003g0090 a0001c0001t0003g0091 others(12): Show |
15 | HG00323.hp2 HG01256.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.591+10938G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70944901 | |||||||
chr6:70945177 | C | A | 1 | a0001c0001t0013g0097 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.591+10662G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945177 | |||||||
chr6:70945204 | C | T | 1 | a0001c0001t0001g0058 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.591+10635G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945204 | |||||||
chr6:70945219 | C | T | 2 | a0001c0002t0008g0249 a0001c0002t0094g0274 |
2 | HG00099.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.591+10620G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945219 | |||||||
chr6:70945220 | A | G | 232 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(229): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(231): Show |
intron_variant | MODIFIER | c.591+10619T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945220 | |||||||
chr6:70945232 | T | C | 2 | a0001c0001t0002g0174 a0001c0001t0013g0129 |
2 | NA18997.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.591+10607A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945232 | |||||||
chr6:70945337 | C | T | 3 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0001t0002g0154 |
3 | HG00544.hp1 NA18965.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.591+10502G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945337 | |||||||
chr6:70945343 | T | C | 1 | a0001c0001t0002g0038 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.591+10496A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945343 | |||||||
chr6:70945390 | A | G | 237 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.591+10449T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945390 | |||||||
chr6:70945582 | A | C | 2 | a0001c0001t0002g0150 a0001c0001t0002g0151 |
2 | HG00408.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.591+10257T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945582 | |||||||
chr6:70945587 | C | A | 1 | a0001c0001t0024g0130 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.591+10252G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945587 | |||||||
chr6:70945806 | T | G | 1 | a0001c0001t0003g0132 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.591+10033A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945806 | |||||||
chr6:70945829 | C | T | 12 | a0001c0002t0011g0269 a0001c0002t0022g0265 a0001c0002t0022g0268 others(9): Show |
12 | HG02132.hp1 HG02135.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.591+10010G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945829 | |||||||
chr6:70945876 | G | A | 1 | a0001c0001t0055g0131 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.591+9963C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945876 | |||||||
chr6:70945967 | A | T | 29 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0012g0023 others(26): Show |
29 | HG00673.hp2 HG01074.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.591+9872T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70945967 | |||||||
chr6:70946074 | A | G | 112 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0144 others(109): Show |
112 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.591+9765T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946074 | |||||||
chr6:70946133 | G | A | 1 | a0001c0001t0004g0099 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.591+9706C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946133 | |||||||
chr6:70946140 | G | A | 39 | a0001c0002t0008g0249 a0001c0002t0011g0254 a0001c0002t0011g0255 others(36): Show |
39 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.591+9699C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946140 | |||||||
chr6:70946168 | C | T | 1 | a0001c0002t0011g0270 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.591+9671G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946168 | |||||||
chr6:70946249 | A | G | 1 | a0001c0001t0003g0132 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.591+9590T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946249 | |||||||
chr6:70946273 | C | T | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+9566G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946273 | |||||||
chr6:70946307 | C | T | 1 | a0001c0001t0002g0038 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.591+9532G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946307 | |||||||
chr6:70946388 | C | T | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+9451G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946388 | |||||||
chr6:70946489 | G | A | 1 | a0001c0001t0066g0143 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.591+9350C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946489 | |||||||
chr6:70946512 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.591+9327T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946512 | |||||||
chr6:70946646 | C | A | 2 | a0001c0002t0011g0261 a0001c0002t0096g0260 |
2 | HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.591+9193G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946646 | |||||||
chr6:70946697 | A | C | 3 | a0001c0002t0030g0262 a0001c0002t0030g0263 a0001c0002t0092g0264 |
3 | NA18951.hp1 NA18962.hp2 NA18984.hp1 |
intron_variant | MODIFIER | c.591+9142T>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946697 | |||||||
chr6:70946726 | C | T | 1 | a0001c0001t0058g0083 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.591+9113G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946726 | |||||||
chr6:70946727 | G | A | 1 | a0001c0001t0003g0139 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.591+9112C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946727 | |||||||
chr6:70946748 | A | G | 3 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0001t0061g0094 |
3 | NA18962.hp1 NA19006.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.591+9091T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946748 | |||||||
chr6:70946760 | C | A | 236 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(233): Show |
238 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.591+9079G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946760 | |||||||
chr6:70946772 | A | G | 237 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.591+9067T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946772 | |||||||
chr6:70946853 | C | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.591+8986G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946853 | |||||||
chr6:70946870 | T | C | 69 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0144 others(66): Show |
69 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.591+8969A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70946870 | |||||||
chr6:70947137 | T | C | 1 | a0001c0002t0007g0184 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.591+8702A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947137 | |||||||
chr6:70947287 | C | T | 13 | a0001c0001t0068g0168 a0001c0002t0011g0269 a0001c0002t0022g0265 others(10): Show |
13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.591+8552G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947287 | |||||||
chr6:70947324 | T | C | 1 | a0001c0002t0098g0292 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.591+8515A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947324 | |||||||
chr6:70947336 | A | G | 1 | a0001c0001t0020g0079 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.591+8503T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947336 | |||||||
chr6:70947344 | T | C | 39 | a0001c0002t0008g0249 a0001c0002t0011g0254 a0001c0002t0011g0255 others(36): Show |
39 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.591+8495A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947344 | |||||||
chr6:70947423 | G | C | 1 | a0001c0001t0057g0074 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.591+8416C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947423 | |||||||
chr6:70947436 | G | A | 2 | a0001c0002t0088g0296 a0001c0002t0089g0297 |
2 | HG02738.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.591+8403C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947436 | |||||||
chr6:70947470 | A | G | 1 | a0001c0002t0040g0185 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.591+8369T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947470 | |||||||
chr6:70947580 | G | C | 25 | a0001c0002t0008g0249 a0001c0002t0014g0278 a0001c0002t0014g0283 others(22): Show |
25 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.591+8259C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947580 | |||||||
chr6:70947585 | A | G | 69 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0144 others(66): Show |
69 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.591+8254T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947585 | |||||||
chr6:70947635 | C | T | 236 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(233): Show |
238 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.591+8204G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947635 | |||||||
chr6:70947654 | A | G | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+8185T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947654 | |||||||
chr6:70947694 | C | G | 29 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0012g0023 others(26): Show |
29 | HG00673.hp2 HG01074.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.591+8145G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947694 | |||||||
chr6:70947746 | C | T | 15 | a0001c0001t0001g0102 a0001c0001t0003g0090 a0001c0001t0003g0091 others(12): Show |
15 | HG00323.hp2 HG01256.hp1 HG01975.hp2 others(12): Show |
intron_variant | MODIFIER | c.591+8093G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947746 | |||||||
chr6:70947760 | C | T | 1 | a0001c0001t0003g0082 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.591+8079G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947760 | |||||||
chr6:70947861 | C | T | 1 | a0001c0001t0019g0018 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.591+7978G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947861 | |||||||
chr6:70947894 | A | G | 237 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.591+7945T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947894 | |||||||
chr6:70947978 | A | G | 237 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.591+7861T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70947978 | |||||||
chr6:70948023 | T | C | 1 | a0001c0002t0008g0247 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.591+7816A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948023 | |||||||
chr6:70948075 | G | A | 1 | a0001c0001t0057g0074 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.591+7764C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948075 | |||||||
chr6:70948108 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.591+7731C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948108 | |||||||
chr6:70948197 | C | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.591+7642G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948197 | |||||||
chr6:70948252 | G | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.591+7587C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948252 | |||||||
chr6:70948313 | G | A | 237 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.591+7526C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948313 | |||||||
chr6:70948325 | G | C | 9 | a0001c0001t0003g0132 a0001c0001t0003g0134 a0001c0001t0003g0136 others(6): Show |
9 | HG01884.hp2 HG02280.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.591+7514C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948325 | |||||||
chr6:70948418 | G | A | 25 | a0001c0002t0008g0249 a0001c0002t0014g0278 a0001c0002t0014g0283 others(22): Show |
25 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(22): Show |
intron_variant | MODIFIER | c.591+7421C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948418 | |||||||
chr6:70948428 | A | G | 3 | a0001c0001t0018g0013 a0001c0001t0018g0014 a0001c0001t0018g0015 |
3 | HG01256.hp2 HG01257.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.591+7411T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948428 | |||||||
chr6:70948434 | A | G | 1 | a0001c0001t0001g0042 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.591+7405T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948434 | |||||||
chr6:70948545 | A | G | 1 | a0001c0002t0007g0184 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.591+7294T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948545 | |||||||
chr6:70948574 | A | G | 1 | a0001c0001t0073g0108 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.591+7265T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948574 | |||||||
chr6:70948591 | C | G | 3 | a0001c0001t0003g0169 a0001c0001t0035g0167 a0001c0001t0064g0166 |
3 | HG01168.hp1 HG01169.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.591+7248G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948591 | |||||||
chr6:70948637 | G | C | 233 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(230): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(232): Show |
intron_variant | MODIFIER | c.591+7202C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948637 | |||||||
chr6:70948749 | A | G | 1 | a0001c0002t0086g0183 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.591+7090T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948749 | |||||||
chr6:70948760 | A | G | 1 | a0001c0001t0034g0107 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.591+7079T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70948760 | |||||||
chr6:70949143 | G | A | 2 | a0001c0001t0017g0008 a0001c0001t0019g0030 |
2 | NA19078.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.591+6696C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949143 | |||||||
chr6:70949190 | C | A | 2 | a0001c0001t0003g0100 a0001c0001t0003g0101 |
2 | HG03669.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.591+6649G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949190 | |||||||
chr6:70949203 | A | G | 69 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0144 others(66): Show |
69 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.591+6636T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949203 | |||||||
chr6:70949258 | G | A | 1 | a0001c0001t0102g0302 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.591+6581C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949258 | |||||||
chr6:70949266 | G | A | 1 | a0001c0002t0011g0269 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.591+6573C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949266 | |||||||
chr6:70949287 | T | A | 1 | a0001c0001t0068g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.591+6552A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949287 | |||||||
chr6:70949290 | T | A | 1 | a0001c0001t0068g0168 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.591+6549A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949290 | |||||||
chr6:70949460 | G | T | 236 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(233): Show |
238 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.591+6379C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949460 | |||||||
chr6:70949581 | T | C | 236 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(233): Show |
238 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(235): Show |
intron_variant | MODIFIER | c.591+6258A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949581 | |||||||
chr6:70949625 | C | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.591+6214G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949625 | |||||||
chr6:70949646 | T | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.591+6193A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949646 | |||||||
chr6:70949713 | C | A | 4 | a0001c0001t0004g0140 a0001c0001t0004g0141 a0001c0001t0036g0142 others(1): Show |
4 | HG02109.hp2 HG03130.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+6126G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70949713 | |||||||
chr6:70950014 | T | C | 1 | a0001c0001t0013g0034 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.591+5825A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950014 | |||||||
chr6:70950039 | C | G | 6 | a0001c0001t0001g0144 a0001c0001t0003g0145 a0001c0001t0003g0146 others(3): Show |
6 | HG00423.hp1 HG02129.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.591+5800G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950039 | |||||||
chr6:70950111 | G | T | 68 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(65): Show |
70 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(67): Show |
intron_variant | MODIFIER | c.591+5728C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950111 | |||||||
chr6:70950134 | G | C | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+5705C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950134 | |||||||
chr6:70950229 | G | T | 1 | a0001c0001t0003g0082 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.591+5610C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950229 | |||||||
chr6:70950299 | AATT | A | 16 | a0001c0001t0012g0023 a0001c0001t0012g0026 a0001c0001t0012g0028 others(13): Show |
16 | HG00673.hp2 HG01074.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.591+5537_591+5539d others(5): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950299 | |||||||
chr6:70950300 | AT | A | 174 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(171): Show |
176 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(173): Show |
intron_variant | MODIFIER | c.591+5538delA | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950300 | |||||||
chr6:70950300 | ATT | A | 29 | a0001c0001t0001g0102 a0001c0001t0002g0038 a0001c0001t0002g0046 others(26): Show |
29 | HG00323.hp2 HG00423.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.591+5537_591+5538d others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950300 | |||||||
chr6:70950301 | T | A | 5 | a0001c0001t0003g0081 a0001c0001t0003g0134 a0001c0001t0013g0117 others(2): Show |
5 | HG02738.hp1 HG03041.hp1 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.591+5538A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950301 | |||||||
chr6:70950302 | T | A | 175 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(172): Show |
177 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.591+5537A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950302 | |||||||
chr6:70950408 | A | G | 224 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.591+5431T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950408 | |||||||
chr6:70950493 | T | C | 8 | a0001c0001t0004g0053 a0001c0001t0004g0057 a0001c0001t0004g0075 others(5): Show |
8 | HG02145.hp2 HG02258.hp2 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.591+5346A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950493 | |||||||
chr6:70950530 | C | T | 112 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(109): Show |
114 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(111): Show |
intron_variant | MODIFIER | c.591+5309G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950530 | |||||||
chr6:70950625 | C | T | 237 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.591+5214G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950625 | |||||||
chr6:70950630 | A | T | 53 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0047 others(50): Show |
54 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(51): Show |
intron_variant | MODIFIER | c.591+5209T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950630 | |||||||
chr6:70950660 | C | G | 1 | a0001c0001t0102g0302 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.591+5179G>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950660 | |||||||
chr6:70950892 | A | G | 6 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0048g0009 others(3): Show |
6 | HG02630.hp2 HG02723.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.591+4947T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70950892 | |||||||
chr6:70951010 | A | G | 2 | a0001c0001t0004g0057 a0001c0001t0024g0041 |
2 | HG02145.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.591+4829T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70951010 | |||||||
chr6:70951049 | G | A | 111 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0144 others(108): Show |
111 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(108): Show |
intron_variant | MODIFIER | c.591+4790C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70951049 | |||||||
chr6:70951147 | C | T | 12 | a0001c0002t0011g0269 a0001c0002t0022g0265 a0001c0002t0022g0268 others(9): Show |
12 | HG02132.hp1 HG02135.hp1 NA18951.hp1 others(9): Show |
intron_variant | MODIFIER | c.591+4692G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70951147 | |||||||
chr6:70951264 | T | C | 1 | a0001c0002t0021g0248 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.591+4575A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70951264 | |||||||
chr6:70951307 | A | G | 69 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0144 others(66): Show |
69 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.591+4532T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70951307 | |||||||
chr6:70951383 | G | A | 1 | a0001c0002t0042g0294 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.591+4456C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70951383 | |||||||
chr6:70951383 | G | C | 1 | a0001c0003t0062g0106 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.591+4456C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70951383 | |||||||
chr6:70951920 | T | C | 5 | a0001c0001t0003g0100 a0001c0001t0003g0101 a0001c0001t0004g0099 others(2): Show |
5 | HG00323.hp2 HG01975.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.591+3919A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70951920 | |||||||
chr6:70951938 | T | C | 61 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0047 others(58): Show |
62 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(59): Show |
intron_variant | MODIFIER | c.591+3901A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70951938 | |||||||
chr6:70951986 | A | T | 224 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.591+3853T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70951986 | |||||||
chr6:70952032 | G | T | 62 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0047 others(59): Show |
63 | HG00099.hp2 HG00597.hp1 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.591+3807C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952032 | |||||||
chr6:70952163 | T | C | 69 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0144 others(66): Show |
69 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.591+3676A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952163 | |||||||
chr6:70952299 | T | C | 39 | a0001c0002t0008g0249 a0001c0002t0011g0254 a0001c0002t0011g0255 others(36): Show |
39 | HG00099.hp1 HG00323.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.591+3540A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952299 | |||||||
chr6:70952332 | T | C | 13 | a0001c0001t0068g0168 a0001c0002t0011g0269 a0001c0002t0022g0265 others(10): Show |
13 | HG02132.hp1 HG02135.hp1 HG06807.hp2 others(10): Show |
intron_variant | MODIFIER | c.591+3507A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952332 | |||||||
chr6:70952500 | T | TA | 29 | a0001c0001t0012g0010 a0001c0001t0012g0011 a0001c0001t0012g0023 others(26): Show |
29 | HG00673.hp2 HG01074.hp1 HG01255.hp1 others(26): Show |
intron_variant | MODIFIER | c.591+3338dupT | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952500 | |||||||
chr6:70952527 | T | C | 1 | a0001c0001t0017g0008 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.591+3312A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952527 | |||||||
chr6:70952579 | G | A | 5 | a0001c0001t0003g0100 a0001c0001t0003g0101 a0001c0001t0004g0099 others(2): Show |
5 | HG00323.hp2 HG01975.hp2 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.591+3260C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952579 | |||||||
chr6:70952583 | G | T | 224 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(221): Show |
226 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(223): Show |
intron_variant | MODIFIER | c.591+3256C>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952583 | |||||||
chr6:70952618 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.591+3221A>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952618 | |||||||
chr6:70952626 | A | G | 69 | a0001c0001t0001g0119 a0001c0001t0001g0123 a0001c0001t0001g0144 others(66): Show |
69 | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.591+3213T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952626 | |||||||
chr6:70952986 | C | T | 1 | a0001c0002t0022g0298 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.591+2853G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952986 | |||||||
chr6:70952990 | C | T | 1 | a0001c0002t0021g0182 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.591+2849G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70952990 | |||||||
chr6:70953006 | G | C | 237 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(234): Show |
239 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(236): Show |
intron_variant | MODIFIER | c.591+2833C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70953006 | |||||||
chr6:70953139 | G | C | 18 | a0001c0001t0001g0144 a0001c0001t0001g0157 a0001c0001t0001g0161 others(15): Show |
18 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(15): Show |
intron_variant | MODIFIER | c.591+2700C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70953139 | |||||||
chr6:70953200 | A | G | 5 | a0001c0001t0001g0102 a0001c0001t0003g0090 a0001c0001t0003g0091 others(2): Show |
5 | NA18940.hp1 NA18962.hp1 NA19005.hp1 others(2): Show |
intron_variant | MODIFIER | c.591+2639T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70953200 | |||||||
chr6:70953495 | A | G | 185 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(182): Show |
187 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.591+2344T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70953495 | |||||||
chr6:70953659 | T | G | 7 | a0001c0001t0001g0055 a0001c0001t0001g0056 a0001c0001t0001g0080 others(4): Show |
7 | HG00099.hp2 HG01433.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.591+2180A>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70953659 | |||||||
chr6:70954016 | G | A | 1 | a0001c0001t0076g0176 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.591+1823C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70954016 | |||||||
chr6:70954246 | T | A | 185 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(182): Show |
187 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.591+1593A>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70954246 | |||||||
chr6:70954749 | C | T | 1 | a0001c0002t0015g0252 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.591+1090G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70954749 | |||||||
chr6:70954854 | A | ACC | 83 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(80): Show |
85 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.591+983_591+984dup others(2): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70954854 | |||||||
chr6:70954915 | C | CG | 25 | a0001c0001t0017g0008 a0001c0002t0005g0181 a0001c0002t0011g0254 others(22): Show |
25 | HG01978.hp2 HG02132.hp1 HG02135.hp1 others(22): Show |
intron_variant | MODIFIER | c.591+923dupC | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70954915 | |||||||
chr6:70954915 | C | CGGG | 37 | a0001c0001t0001g0058 a0001c0001t0001g0061 a0001c0001t0001g0063 others(34): Show |
38 | HG00673.hp1 HG01975.hp1 HG01993.hp1 others(35): Show |
intron_variant | MODIFIER | c.591+921_591+923dup others(3): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70954915 | |||||||
chr6:70954915 | C | CGGGG | 22 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0047 others(19): Show |
22 | HG00099.hp2 HG00597.hp1 HG01168.hp1 others(19): Show |
intron_variant | MODIFIER | c.591+920_591+923dup others(4): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70954915 | |||||||
chr6:70954918 | G | A | 4 | a0001c0001t0004g0162 a0001c0001t0004g0164 a0001c0001t0004g0165 others(1): Show |
4 | HG02109.hp1 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+921C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70954918 | |||||||
chr6:70954923 | G | C | 4 | a0001c0001t0036g0105 a0001c0001t0045g0004 a0001c0001t0069g0104 others(1): Show |
4 | HG02559.hp1 HG02717.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+916C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70954923 | |||||||
chr6:70955175 | C | CA | 18 | a0001c0001t0002g0038 a0001c0001t0003g0036 a0001c0001t0003g0103 others(15): Show |
18 | HG01167.hp1 HG02280.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.591+663dupT | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955175 | |||||||
chr6:70955175 | C | CAA | 161 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0047 others(158): Show |
162 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(159): Show |
intron_variant | MODIFIER | c.591+662_591+663dup others(2): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955175 | |||||||
chr6:70955175 | C | CAAA | 11 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0170 others(8): Show |
12 | HG01168.hp1 HG01169.hp2 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.591+661_591+663dup others(3): Show |
B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955175 | |||||||
chr6:70955208 | A | T | 1 | a0001c0001t0002g0035 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.591+631T>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955208 | |||||||
chr6:70955223 | G | C | 4 | a0001c0002t0022g0298 a0001c0002t0029g0299 a0001c0002t0030g0301 others(1): Show |
4 | HG02132.hp1 NA18981.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.591+616C>G | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955223 | |||||||
chr6:70955269 | C | T | 1 | a0001c0001t0013g0034 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.591+570G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955269 | |||||||
chr6:70955296 | C | T | 77 | a0001c0001t0001g0042 a0001c0001t0001g0044 a0001c0001t0001g0047 others(74): Show |
78 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.591+543G>A | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955296 | |||||||
chr6:70955639 | C | A | 1 | a0001c0001t0012g0031 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.591+200G>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955639 | |||||||
chr6:70955769 | G | A | 1 | a0001c0001t0002g0174 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.591+70C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955769 | |||||||
chr6:70955770 | A | G | 186 | a0001c0001t0001g0002 a0001c0001t0001g0042 a0001c0001t0001g0044 others(183): Show |
188 | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.591+69T>C | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955770 | |||||||
chr6:70955776 | G | A | 95 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0119 others(92): Show |
96 | HG00323.hp2 HG00408.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.591+63C>T | B3GAT2 | ENSG00000112309.11 | transcript | ENST00000230053.11 | protein_coding | 1/3 | chr6 | 70955776 |